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rs276174861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;CC) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs276174861(-;-)
Make rs276174861(CC;CC)
ReferenceGRCh38 38.1/142
Chromosome13
Position32340010
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174861
ebirs276174861
HLIrs276174861
Exacrs276174861
Varsomers276174861
Maprs276174861
PheGenIrs276174861
hapmaprs276174861
1000 genomesrs276174861
hgdprs276174861
ensemblrs276174861
gopubmedrs276174861
geneviewrs276174861
scholarrs276174861
googlers276174861
pharmgkbrs276174861
gwascentralrs276174861
openSNPrs276174861
23andMers276174861
23andMe allrs276174861
SNP Nexus

SNPshotrs276174861
SNPdbers276174861
MSV3drs276174861
GWAS Ctlgrs276174861
Max Magnitude6
rs276174861, also known as 5883insCC, c.5655_5656insCC and p.Cys1885_Gln1886?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174861(CC;CC)
Alt rs276174861(CC;CC)
Reference rs276174861(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914147_32914148insCC
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113454.1,