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rs276174857

From SNPedia

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


Make rs276174857(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326521
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174857
ebirs276174857
HLIrs276174857
Exacrs276174857
Varsomers276174857
Maprs276174857
PheGenIrs276174857
hapmaprs276174857
1000 genomesrs276174857
hgdprs276174857
ensemblrs276174857
gopubmedrs276174857
geneviewrs276174857
scholarrs276174857
googlers276174857
pharmgkbrs276174857
gwascentralrs276174857
openSNPrs276174857
23andMers276174857
23andMe allrs276174857
SNP Nexus

SNPshotrs276174857
SNPdbers276174857
MSV3drs276174857
GWAS Ctlgrs276174857
Max Magnitude6
rs276174857, also known as 767delT, c.539_539delT and p.Ile180=fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174857(;)
Alt rs276174857(;)
Reference rs276174857(T;T)
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.32900658delT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044651.2, RCV000113763.1,