RS782531869 VMA12

Health Risk Chr 17:28357762
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What This Variant Does
"CLNSIG=5
Associated Conditions
TMEM199-CDG
Congenital disorders of glycosylation type II
TMEM199-related disorder
TMEM199-CDG
Congenital disorders of glycosylation type II
TMEM199-related disorder
Other Variants in VMA12
rs369488804 rs869025586 rs869025587 rs781939580 rs782563182 rs139239352
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