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

rs398122556

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACTT;ACTT) 0 common in clinvar
(CTTA;CTTA) 0 common in clinvar
Make rs398122556(-;-)
Make rs398122556(-;CTTA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340760
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122556
ebirs398122556
HLIrs398122556
Exacrs398122556
Varsomers398122556
Maprs398122556
PheGenIrs398122556
hapmaprs398122556
1000 genomesrs398122556
hgdprs398122556
ensemblrs398122556
gopubmedrs398122556
geneviewrs398122556
scholarrs398122556
googlers398122556
pharmgkbrs398122556
gwascentralrs398122556
openSNPrs398122556
23andMers398122556
23andMe allrs398122556
SNP Nexus

SNPshotrs398122556
SNPdbers398122556
MSV3drs398122556
GWAS Ctlgrs398122556
Max Magnitude0
ClinVar
Risk rs398122556(;)
Alt rs398122556(;)
Reference rs398122556(ACTT;ACTT)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914897_32914900delCTTA
CLNSRC ClinVar
CLNACC RCV000076965.2,