RS202156896 ERCC2

Health Risk Chr 19:45369097
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Associated Conditions
Xeroderma pigmentosum
group D
Inborn genetic diseases
Xeroderma pigmentosum
group D
Inborn genetic diseases
Other Variants in ERCC2
rs121913016 rs121913017 rs121913018 rs121913019 rs121913020 rs121913021 rs121913023 rs121913024 rs2123229159 rs121913025
Ask Dr. Hemsworth about this variant