RS72552255 ATP7B

Health Risk Chr 13:51946414
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What This Variant Does
"CLNSIG=5
Associated Conditions
Wilson disease
Inborn genetic diseases
ATP7B-related disorder
Hearing loss
autosomal recessive 109
Wilson disease
Inborn genetic diseases
ATP7B-related disorder
Hearing loss
autosomal recessive 109
Other Variants in ATP7B
rs76151636 rs121907992 rs137853280 rs121907994 rs28942074 rs2138570625 rs28942075 rs28942076 rs121907993 rs121907990
Ask Dr. Hemsworth about this variant