RS41556519 ERCC2

Health Risk Chr 19:45352352
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What This Variant Does
"CLNSIG=5
Associated Conditions
Xeroderma pigmentosum
group D
Inborn genetic diseases
Cerebrooculofacioskeletal syndrome 2
Trichothiodystrophy 1
photosensitive
Hereditary cancer-predisposing syndrome
Xeroderma pigmentosum
group D
Inborn genetic diseases
Cerebrooculofacioskeletal syndrome 2
Trichothiodystrophy 1
photosensitive
Hereditary cancer-predisposing syndrome
Other Variants in ERCC2
rs121913016 rs121913017 rs121913018 rs121913019 rs121913020 rs121913021 rs121913023 rs121913024 rs2123229159 rs121913025
Ask Dr. Hemsworth about this variant