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rs80359664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;CT) 6 BRCA2 variant considered pathogenic for breast cancer
(CT;CT) 0 common in clinvar
(TC;TC) 0 common in clinvar


Make rs80359664(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356559
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359664
ebirs80359664
HLIrs80359664
Exacrs80359664
Varsomers80359664
Maprs80359664
PheGenIrs80359664
hapmaprs80359664
1000 genomesrs80359664
hgdprs80359664
ensemblrs80359664
gopubmedrs80359664
geneviewrs80359664
scholarrs80359664
googlers80359664
pharmgkbrs80359664
gwascentralrs80359664
openSNPrs80359664
23andMers80359664
23andMe allrs80359664
SNP Nexus

SNPshotrs80359664
SNPdbers80359664
MSV3drs80359664
GWAS Ctlgrs80359664
Max Magnitude6
rs80359664, also known as 7795delCT, c.7567_7568delCT and p.Leu2523Glufs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359664(;)
Alt rs80359664(;)
Reference rs80359664(TC;TC)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32930696_32930697delCT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031687.4, RCV000045250.2,