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

rs398122576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122576(-;-)
Make rs398122576(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32354995
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122576
ebirs398122576
HLIrs398122576
Exacrs398122576
Varsomers398122576
Maprs398122576
PheGenIrs398122576
hapmaprs398122576
1000 genomesrs398122576
hgdprs398122576
ensemblrs398122576
gopubmedrs398122576
geneviewrs398122576
scholarrs398122576
googlers398122576
pharmgkbrs398122576
gwascentralrs398122576
openSNPrs398122576
23andMers398122576
23andMe allrs398122576
SNP Nexus

SNPshotrs398122576
SNPdbers398122576
MSV3drs398122576
GWAS Ctlgrs398122576
Max Magnitude0
ClinVar
Risk rs398122576(;)
Alt rs398122576(;)
Reference rs398122576(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32929132delC
CLNSRC ClinVar
CLNACC RCV000076988.2,