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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129929467, PRDM2
(A1273T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129929467, PRDM2
(P1285S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
LOC129929467, PRDM2
(K1295R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129929467, PRDM2
(S1501A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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