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rs276174848

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs276174848(-;-)
Make rs276174848(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326154
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174848
ebirs276174848
HLIrs276174848
Exacrs276174848
Varsomers276174848
Maprs276174848
PheGenIrs276174848
hapmaprs276174848
1000 genomesrs276174848
hgdprs276174848
ensemblrs276174848
gopubmedrs276174848
geneviewrs276174848
scholarrs276174848
googlers276174848
pharmgkbrs276174848
gwascentralrs276174848
openSNPrs276174848
23andMers276174848
23andMe allrs276174848
SNP Nexus

SNPshotrs276174848
SNPdbers276174848
MSV3drs276174848
GWAS Ctlgrs276174848
Max Magnitude0
ClinVar
Risk rs276174848(;)
Alt rs276174848(;)
Reference rs276174848(T;T)
Significance Other
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32900291delT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031502.6, RCV000044485.2,