RS773935389 ARSL

Health Risk Chr X:2946055
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Associated Conditions
Chondrodysplasia punctata
brachytelephalangic
autosomal
Inborn genetic diseases
Chondrodysplasia punctata
brachytelephalangic
autosomal
Inborn genetic diseases
Other Variants in ARSL
rs122460152 rs122460153 rs80338711 rs122460154 rs122460155 rs28935474 rs80338714 rs80338710 rs145946864 rs886041135
Ask Dr. Hemsworth about this variant