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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129999418, WDR91
(Y634C +3 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
LOC129999418, WDR91
(A616V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129999418, WDR91
(C622W +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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