Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs886037801
rs886037801
1.000 0.200 13 32337354 frameshift variant T/-;TT delins
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs886037801
rs886037801
1.000 0.200 13 32337354 frameshift variant T/-;TT delins
Hereditary Breast and Ovarian Cancer Syndrome
0.700 0