RS121913047 ERCC3

Health Risk Chr 2:127286772
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What This Variant Does
"[OMIM:?]
Associated Conditions
Xeroderma pigmentosum group B
Inborn genetic diseases
Trichothiodystrophy 2
photosensitive
Xeroderma pigmentosum group B
Inborn genetic diseases
Trichothiodystrophy 2
photosensitive
Other Variants in ERCC3
rs200733704 rs121913045 rs121913046 rs866379139 rs121913048 rs1558964705 rs568193912 rs145201970 rs587778281 rs34295337
Ask Dr. Hemsworth about this variant