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

rs398122559

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs398122559(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340842
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122559
dbSNP (old)rs398122559
ClinGenrs398122559
ebirs398122559
HLIrs398122559
Exacrs398122559
Gnomadrs398122559
Varsomers398122559
Maprs398122559
PheGenIrs398122559
Biobankrs398122559
1000 genomesrs398122559
hgdprs398122559
ensemblrs398122559
gopubmedrs398122559
geneviewrs398122559
scholarrs398122559
googlers398122559
pharmgkbrs398122559
gwascentralrs398122559
openSNPrs398122559
23andMers398122559
23andMe allrs398122559
SNP Nexus

SNPshotrs398122559
SNPdbers398122559
MSV3drs398122559
GWAS Ctlgrs398122559
Max Magnitude6
ClinVar
Risk rs398122559(T;T)
Alt rs398122559(T;T)
Reference Rs398122559(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32914979C>T
CLNSRC ClinVar
CLNACC RCV000076968.3, RCV000483318.1,