RS4986852 BRCA1

Health Risk Chr 17:43092411 snv missense variant
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What This Variant Does
"rs4986852 is a SNP causing an amino acid change in the breast cancer 1 BRCA1 gene at amino position ...
Associated Conditions
Population Frequencies
gnomAD ALL
0%
1kG AFR
99.8%
1kG ALL
99%
1kG AMR
98%
1kG EAS
100%
1kG EUR
2.9%
1kG SAS
99.7%
Other Variants in BRCA1
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