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Items: 1 to 100 of 2398

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+2 more
GBenign
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+2 more
GBenign
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GUncertain significance
FLCN
Duplication
(3 prime UTR variant)
Spontaneous pneumothorax
+1 more
GBenign
FLCN
Duplication
(3 prime UTR variant)
Spontaneous pneumothorax
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GBenign
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GBenign
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GBenign/Likely benign
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GUncertain significance
FLCN
Deletion
(3 prime UTR variant)
Spontaneous pneumothorax
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
not provided
+2 more
GConflicting classifications of pathogenicity
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+2 more
GBenign
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GConflicting classifications of pathogenicity
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GBenign/Likely benign
FLCN
Single nucleotide variant
(3 prime UTR variant)
not provided
+2 more
GBenign/Likely benign
FLCN
Single nucleotide variant
(3 prime UTR variant)
not provided
+2 more
GBenign
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+2 more
GBenign/Likely benign
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GConflicting classifications of pathogenicity
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+2 more
GBenign
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+2 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
not provided
GLikely benign
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Familial spontaneous pneumothorax
+1 more
GConflicting classifications of pathogenicity
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
not specified
GBenign/Likely benign
FLCN
Deletion
Birt-Hogg-Dube syndrome
GPathogenic
FLCN
Duplication
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Duplication
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Deletion
Birt-Hogg-Dube syndrome
GPathogenic
FLCN
Duplication
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Duplication
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Duplication
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
FLCN
Single nucleotide variant
(3 prime UTR variant)
Birt-Hogg-Dube syndrome
+2 more
GConflicting classifications of pathogenicity
FLCN
Single nucleotide variant
(3 prime UTR variant)
not specified
GLikely benign
FLCN
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FLCN
Deletion
Familial spontaneous pneumothorax
GPathogenic
FLCN
(N579K +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
Birt-Hogg-Dube syndrome
GLikely benign
FLCN
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
FLCN
(R578Q +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
+5 more
GUncertain significance
FLCN
(R596W +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
+2 more
GConflicting classifications of pathogenicity
FLCN
(S595F +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Indel
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
FLCN
(S595A +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
FLCN
(S577P +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
FLCN
(E576D +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
(E576G +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
(E576Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
FLCN
(S575L +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
(S575P +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
FLCN
(A592V +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
(A574T +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FLCN
(T573I +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
(T573S +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
(T573A +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
FLCN
(T573fs +1 more)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
FLCN
(P572H +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GUncertain significance
FLCN
(P590S +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
(P572A +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
FLCN
Duplication
(nonsense +1 more)
Birt-Hogg-Dube syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
Birt-Hogg-Dube syndrome
GLikely benign
FLCN
(R588L +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome 1
+6 more
GConflicting classifications of pathogenicity
FLCN
(R570H +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
FLCN
(R570C +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
Birt-Hogg-Dube syndrome
+1 more
GLikely benign
FLCN
(V569A +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
FLCN
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
FLCN
(T568R +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
(T568M +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
FLCN
(T568A +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
FLCN
(S567F +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome 1
+4 more
GConflicting classifications of pathogenicity
FLCN
(M566I +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
(M566T +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome 1
+3 more
GUncertain significance
FLCN
(M584V +1 more)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
Birt-Hogg-Dube syndrome
GLikely benign
FLCN
(L583F +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
FLCN
(H564Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
FLCN
Single nucleotide variant
(synonymous variant)
not specified
+7 more
GBenign/Likely benign
FLCN
(H582P +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
FLCN
(H564L +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
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