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

rs398122746

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122746(G;T)
Make rs398122746(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336723
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122746
ebirs398122746
HLIrs398122746
Exacrs398122746
Varsomers398122746
Maprs398122746
PheGenIrs398122746
hapmaprs398122746
1000 genomesrs398122746
hgdprs398122746
ensemblrs398122746
gopubmedrs398122746
geneviewrs398122746
scholarrs398122746
googlers398122746
pharmgkbrs398122746
gwascentralrs398122746
openSNPrs398122746
23andMers398122746
23andMe allrs398122746
SNP Nexus

SNPshotrs398122746
SNPdbers398122746
MSV3drs398122746
GWAS Ctlgrs398122746
Max Magnitude0
ClinVar
Risk rs398122746(A,T;A,T)
Alt rs398122746(A,T;A,T)
Reference rs398122746(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.32910860G>T
CLNSRC ClinVar
CLNACC RCV000077684.2,