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Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR76
(A38S)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WDR76
(A52S)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
WDR76
(T118A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(I106T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(S165T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(L239F +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(K203R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(G204R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(I252V +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
WDR76
(V332A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
WDR76
(P284H +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(N372S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(L534F +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(C498S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(R509Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(H578R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(E515A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(L528F +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(V531L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(R605W +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(I543S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WDR76
(N612T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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