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Links from MedGen

Items: 1 to 100 of 602

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C1QTNF5, MFRP
(R201L)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(V471M)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(E496K)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(C454W)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
MFRP, C1QTNF5
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(S193fs)
Microsatellite
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GPathogenic
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(F155L)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Deletion
(intron variant)
Isolated microphthalmia 5
GBenign
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(N167fs)
Duplication
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GPathogenic
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(N304fs)
Duplication
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GPathogenic
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
MFRP, C1QTNF5
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(splice donor variant)
Isolated microphthalmia 5
GPathogenic
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
MFRP, C1QTNF5
(S502fs)
Deletion
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GPathogenic
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+1 more
GLikely benign
ABCG4, APOA1
+72 more
Duplication
Immunodeficiency 19
+5 more
GUncertain significance
C1QTNF5, MFRP
(G217E)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(N167fs)
Deletion
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GPathogenic
C1QTNF5, MFRP
(G476S)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
MFRP, C1QTNF5
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(R57Q)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(A181T)
Inversion
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
MFRP, C1QTNF5
(K505Q)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(D445fs)
Microsatellite
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GPathogenic
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(T115P)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(M253T)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(G288S)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(P382S)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(P221T)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(Q319P)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
+1 more
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(S196F)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(G378R)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(I339V)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(S122P)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(A545V)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(H384fs)
Deletion
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GPathogenic
C1QTNF5, MFRP
(T118I)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
MFRP, C1QTNF5
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(P165A)
Indel
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(N284S)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(G281A)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(V333M)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(E495A)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(G476A)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(P208A)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
MFRP, C1QTNF5
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(A409D)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(F65S)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(N486K)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(S16L)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(L148R)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
(C354Y)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
Single nucleotide variant
(intron variant)
Isolated microphthalmia 5
GLikely benign
C1QTNF5, MFRP
(Q93H)
Single nucleotide variant
(5 prime UTR variant +1 more)
Isolated microphthalmia 5
GUncertain significance
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