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rs398122623

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122623(-;-)
Make rs398122623(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32398337
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122623
ebirs398122623
HLIrs398122623
Exacrs398122623
Varsomers398122623
Maprs398122623
PheGenIrs398122623
hapmaprs398122623
1000 genomesrs398122623
hgdprs398122623
ensemblrs398122623
gopubmedrs398122623
geneviewrs398122623
scholarrs398122623
googlers398122623
pharmgkbrs398122623
gwascentralrs398122623
openSNPrs398122623
23andMers398122623
23andMe allrs398122623
SNP Nexus

SNPshotrs398122623
SNPdbers398122623
MSV3drs398122623
GWAS Ctlgrs398122623
Max Magnitude0
ClinVar
Risk rs398122623(;)
Alt rs398122623(;)
Reference rs398122623(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32972474delG
CLNSRC ClinVar
CLNACC RCV000077052.2,