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rs276174862

From SNPedia

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


Make rs276174862(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340073
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174862
ebirs276174862
HLIrs276174862
Exacrs276174862
Varsomers276174862
Maprs276174862
PheGenIrs276174862
hapmaprs276174862
1000 genomesrs276174862
hgdprs276174862
ensemblrs276174862
gopubmedrs276174862
geneviewrs276174862
scholarrs276174862
googlers276174862
pharmgkbrs276174862
gwascentralrs276174862
openSNPrs276174862
23andMers276174862
23andMe allrs276174862
SNP Nexus

SNPshotrs276174862
SNPdbers276174862
MSV3drs276174862
GWAS Ctlgrs276174862
Max Magnitude6
rs276174862, also known as 5946delCTCT, c.5718_5721delCTCT and p.Asn1906_Ser1907?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174862(;)
Alt rs276174862(;)
Reference rs276174862(CTCT;CTCT)
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.32914210_32914213delCTCT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044727.2, RCV000113469.1,