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rs80359705

From SNPedia

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


Make rs80359705(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363499
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359705
ebirs80359705
HLIrs80359705
Exacrs80359705
Varsomers80359705
Maprs80359705
PheGenIrs80359705
hapmaprs80359705
1000 genomesrs80359705
hgdprs80359705
ensemblrs80359705
gopubmedrs80359705
geneviewrs80359705
scholarrs80359705
googlers80359705
pharmgkbrs80359705
gwascentralrs80359705
openSNPrs80359705
23andMers80359705
23andMe allrs80359705
SNP Nexus

SNPshotrs80359705
SNPdbers80359705
MSV3drs80359705
GWAS Ctlgrs80359705
Max Magnitude6
rs80359705, also known as 8525delC, c.8297_8297delC and p.Thr2766Asnfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs80359705(;)
Alt rs80359705(;)
Reference rs80359705(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome not provided Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome not provided Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1
Reversed 0
HGVS NC_000013.10:g.32937636delC
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031732.6, RCV000034463.3, RCV000045466.5, RCV000163359.1, RCV000210122.1,