RS80338714 ARSL

Health Risk Chr X:2934859
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What This Variant Does
"[OMIM:?]
Associated Conditions
X-linked chondrodysplasia punctata 1
See cases
Chondrodysplasia punctata
brachytelephalangic
autosomal
Inborn genetic diseases
X-linked chondrodysplasia punctata 1
See cases
Chondrodysplasia punctata
brachytelephalangic
autosomal
Inborn genetic diseases
Other Variants in ARSL
rs122460152 rs122460153 rs80338711 rs122460154 rs122460155 rs28935474 rs80338710 rs145946864 rs886041135 rs886041134
Ask Dr. Hemsworth about this variant