Have questions? Visit https://www.reddit.com/r/SNPedia

rs276174915

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGATTCAGGT;AAGATTCAGGT) 0 common in clinvar
Make rs276174915(-;-)
Make rs276174915(-;ATTCAGGTAAG)
Make rs276174915(ATTCAGGTAAG;ATTCAGGTAAG)
ReferenceGRCh38 38.1/142
Chromosome13
Position32379510
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174915
dbSNP (old)rs276174915
ClinGenrs276174915
ebirs276174915
HLIrs276174915
Exacrs276174915
Gnomadrs276174915
Varsomers276174915
Maprs276174915
PheGenIrs276174915
Biobankrs276174915
1000 genomesrs276174915
hgdprs276174915
ensemblrs276174915
gopubmedrs276174915
geneviewrs276174915
scholarrs276174915
googlers276174915
pharmgkbrs276174915
gwascentralrs276174915
openSNPrs276174915
23andMers276174915
23andMe allrs276174915
SNP Nexus

SNPshotrs276174915
SNPdbers276174915
MSV3drs276174915
GWAS Ctlgrs276174915
Max Magnitude0
ClinVar
Risk rs276174915(-;-)
Alt rs276174915(-;-)
Reference Rs276174915(AAGATTCAGGT;AAGATTCAGGT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome not provided Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32953647_32953657delATTCAGGTAAG
CLNSRC Ambry Genetics
CLNACC RCV000129964.2, RCV000236901.1, RCV000238747.2,