RS143153871 XRCC2

Health Risk Chr 7:152648842
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What This Variant Does
"CLNSIG=5
Associated Conditions
Fanconi anemia complementation group U
Hereditary cancer-predisposing syndrome
Short stature
microcephaly
and endocrine dysfunction
Fanconi anemia complementation group U
Hereditary cancer-predisposing syndrome
Short stature
microcephaly
and endocrine dysfunction
Other Variants in XRCC2
rs140214637 rs587780129 rs61762969 rs368445278 rs149186933 rs56103026 rs149099078 rs730882046 rs730882040 rs730882048
Ask Dr. Hemsworth about this variant