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rs276174839

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;GG) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs276174839(-;-)
Make rs276174839(GG;GG)
ReferenceGRCh38 38.1/142
Chromosome13
Position32338369
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174839
ebirs276174839
HLIrs276174839
Exacrs276174839
Varsomers276174839
Maprs276174839
PheGenIrs276174839
hapmaprs276174839
1000 genomesrs276174839
hgdprs276174839
ensemblrs276174839
gopubmedrs276174839
geneviewrs276174839
scholarrs276174839
googlers276174839
pharmgkbrs276174839
gwascentralrs276174839
openSNPrs276174839
23andMers276174839
23andMe allrs276174839
SNP Nexus

SNPshotrs276174839
SNPdbers276174839
MSV3drs276174839
GWAS Ctlgrs276174839
Max Magnitude6
rs276174839, also known as 4242insGG, c.4014_4015insGG and p.Gly1338_Ser1339?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174839(GG;GG)
Alt rs276174839(GG;GG)
Reference rs276174839(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912506_32912507insGG
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113260.1,