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rs276174916

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTT;GTT) 0 common in clinvar
Make rs276174916(AA;AA)
Make rs276174916(AA;GTT)
ReferenceGRCh38 38.1/142
Chromosome13
Position32379749
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174916
ebirs276174916
HLIrs276174916
Exacrs276174916
Varsomers276174916
Maprs276174916
PheGenIrs276174916
hapmaprs276174916
1000 genomesrs276174916
hgdprs276174916
ensemblrs276174916
gopubmedrs276174916
geneviewrs276174916
scholarrs276174916
googlers276174916
pharmgkbrs276174916
gwascentralrs276174916
openSNPrs276174916
23andMers276174916
23andMe allrs276174916
SNP Nexus

SNPshotrs276174916
SNPdbers276174916
MSV3drs276174916
GWAS Ctlgrs276174916
Max Magnitude0
ClinVar
Risk rs276174916(AA;AA)
Alt rs276174916(AA;AA)
Reference rs276174916(GTT;GTT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32953886_32953888delGTTinsAA
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000130922.2,