RS797044891 TIMM50

Health Risk Chr 19:39488169
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
3-methylglutaconic aciduria type 9
Inborn genetic diseases
3-methylglutaconic aciduria type 9
Other Variants in TIMM50
rs1244226820 rs1305711807 rs1449758112 rs776019250 rs35135520 rs11545196 rs1166132682 rs368335134 rs1457024558 rs760304945
Ask Dr. Hemsworth about this variant