RS397509199 BRCA1

Health Risk Chr 17:43071077
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What This Variant Does
"rs397509199, also known as c.4837delA and p.Ser1613Valfs, is considered a pathogenic BRCA1 gene muta...
Associated Conditions
Breast-ovarian cancer
familial
susceptibility to
1
Hereditary breast ovarian cancer syndrome
Breast-ovarian cancer
familial
susceptibility to
1
Hereditary breast ovarian cancer syndrome
Other Variants in BRCA1
rs80357064 rs28897672 rs80357914 rs80359874 rs80357780 rs80357971 rs80357601 rs62625308 rs28897686 rs80357868
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