RS758398497 ARSL

Health Risk Chr X:2938119
Upload your DNA to see your genotype for this variant.
Associated Conditions
X-linked chondrodysplasia punctata 1
Inborn genetic diseases
Chondrodysplasia punctata
brachytelephalangic
autosomal
X-linked chondrodysplasia punctata 1
Inborn genetic diseases
Chondrodysplasia punctata
brachytelephalangic
autosomal
Other Variants in ARSL
rs122460152 rs122460153 rs80338711 rs122460154 rs122460155 rs28935474 rs80338714 rs80338710 rs145946864 rs886041135
Ask Dr. Hemsworth about this variant