RS144564120 ERCC2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mixed Phenotype Acute Leukemia
T/Myeloid
Not Otherwise Specified
ERCC2-related disorder
Xeroderma pigmentosum
group D
Trichothiodystrophy 1
photosensitive
Inborn genetic diseases
Cerebrooculofacioskeletal syndrome 2
Cervical cancer
Familial cancer of breast
Colon adenocarcinoma
Ovarian serous cystadenocarcinoma
Melanoma
Other Variants in ERCC2