RS121908700 CHEK2

Health Risk Chr 22:28725371 snv splice region variant
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Associated Conditions
Hereditary cancer-predisposing syndrome
Familial cancer of breast
CHEK2-related cancer predisposition
Breast and/or ovarian cancer
Hereditary cancer
CHEK2-related disorder
Acute myeloid leukemia
Hereditary cancer-predisposing syndrome
Familial cancer of breast
Hereditary cancer-predisposing syndrome
Familial cancer of breast
CHEK2-related cancer predisposition
Breast and/or ovarian cancer
Hereditary cancer
CHEK2-related disorder
Population Frequencies
gnomAD ALL
99.9%
1kG AFR
100%
1kG ALL
99.9%
1kG AMR
0.1%
1kG EAS
100%
1kG EUR
99.7%
1kG SAS
100%
Other Variants in CHEK2
rs17879961 rs137853007 rs2145785282 rs137853008 rs137853009 rs137853010 rs121908701 rs121908702 rs137853011 rs121908695
Ask Dr. Hemsworth about this variant