RS2135904246 STT3A

Health Risk Chr 11:125597107
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Associated Conditions
Congenital disorder of glycosylation
type Iw
autosomal dominant
Congenital disorder of glycosylation
type Iw
autosomal dominant
Other Variants in STT3A
rs587777216 rs2135921186 rs2135938300 rs780062429 rs759953502
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