RS376556895 ERCC2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Xeroderma pigmentosum
group D
Cerebrooculofacioskeletal syndrome 2
Trichothiodystrophy 1
photosensitive
Inborn genetic diseases
Hereditary cancer-predisposing syndrome
Trichothiodystrophy 1
photosensitive
Xeroderma pigmentosum
Cerebrooculofacioskeletal syndrome 2
ERCC2-related disorder
group D
Xeroderma pigmentosum
group D
Other Variants in ERCC2