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rs80359658

From SNPedia

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


Make rs80359658(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356535
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359658
ebirs80359658
HLIrs80359658
Exacrs80359658
Varsomers80359658
Maprs80359658
PheGenIrs80359658
hapmaprs80359658
1000 genomesrs80359658
hgdprs80359658
ensemblrs80359658
gopubmedrs80359658
geneviewrs80359658
scholarrs80359658
googlers80359658
pharmgkbrs80359658
gwascentralrs80359658
openSNPrs80359658
23andMers80359658
23andMe allrs80359658
SNP Nexus

SNPshotrs80359658
SNPdbers80359658
MSV3drs80359658
GWAS Ctlgrs80359658
Max Magnitude6
rs80359658, also known as 7771delA, c.7543_7543delA and p.Thr2515Hisfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359658(;)
Alt rs80359658(;)
Reference rs80359658(A;A)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32930672delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045241.2, RCV000113774.1,