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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129937608, SRPRB
(G16V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937608, SRPRB
(G17V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937608, SRPRB
(V40A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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