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Items: 57

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VWA3B
(S7F)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(I55F)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(P62S)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(Y67H)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(P74S)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(G93C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(Y119H)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(R131W)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(L146R)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(R160Q)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely benign
VWA3B
(M165V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(V213I)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(E219V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(G230R)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(S237T)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(I278T)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
LOC126806278, VWA3B
(V302A)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(D336G)
Single nucleotide variant
(5 prime UTR variant +2 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(V340I)
Single nucleotide variant
(5 prime UTR variant +2 more)
Inborn genetic diseases
GLikely benign
VWA3B
(V366M +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(E379Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(A418T +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(V421F +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(P428L +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(S93G +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(S133C +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
VWA3B
(W149R +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(N567D +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(R233G +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(E272V +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(R623H +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(F644Y +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(M704I +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(D740N +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(N405S +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
VWA3B
(K422E +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(R459Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely benign
VWA3B
(M811T +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(T829M +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(W505R +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(V536I +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GLikely benign
VWA3B
(N557S +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(S638L +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(V1054I +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(V711F +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(R1061H +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(M1088V +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(P1091L +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(Y1112H +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(A1115D +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(I773V +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(K1150Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(P868L +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(S1260G +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(P1268S +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(P1270R +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
VWA3B
(L1278V +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
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