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rs276174811

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs276174811(-;-)
Make rs276174811(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position32333085
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174811
ebirs276174811
HLIrs276174811
Exacrs276174811
Varsomers276174811
Maprs276174811
PheGenIrs276174811
hapmaprs276174811
1000 genomesrs276174811
hgdprs276174811
ensemblrs276174811
gopubmedrs276174811
geneviewrs276174811
scholarrs276174811
googlers276174811
pharmgkbrs276174811
gwascentralrs276174811
openSNPrs276174811
23andMers276174811
23andMe allrs276174811
SNP Nexus

SNPshotrs276174811
SNPdbers276174811
MSV3drs276174811
GWAS Ctlgrs276174811
Max Magnitude6
rs276174811, also known as 1835insT, c.1607_1608insT and p.Ser536?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174811(T;T)
Alt rs276174811(T;T)
Reference rs276174811(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907223dupT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000112942.1,