RS143710107 ERCC2

Health Risk Chr 19:45357670
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Associated Conditions
Xeroderma pigmentosum
Inborn genetic diseases
Cerebrooculofacioskeletal syndrome 2
Trichothiodystrophy 1
photosensitive
group D
Xeroderma pigmentosum
Inborn genetic diseases
Cerebrooculofacioskeletal syndrome 2
Trichothiodystrophy 1
photosensitive
group D
Other Variants in ERCC2
rs121913016 rs121913017 rs121913018 rs121913019 rs121913020 rs121913021 rs121913023 rs121913024 rs2123229159 rs121913025
Ask Dr. Hemsworth about this variant