RS137853283 ATP7B

Health Risk Chr 13:51958330
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What This Variant Does
"CLNSIG=5
Associated Conditions
Wilson disease
Inborn genetic diseases
Wilson disease
Inborn genetic diseases
Other Variants in ATP7B
rs76151636 rs121907992 rs137853280 rs121907994 rs28942074 rs2138570625 rs28942075 rs28942076 rs121907993 rs121907990
Ask Dr. Hemsworth about this variant