RS4148353 ABCC1

Health Risk Chr 16:16077290 snv intron variant

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What This Variant Does

"CLNSIG=255

Associated Conditions

Familial cancer of breast

Population Frequencies

1kG AFR

5.6%

1kG ALL

88.2%

1kG AMR

9.1%

1kG EAS

91%

1kG EUR

14.3%

1kG SAS

77.6%

Other Variants in ABCC1