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rs398122593

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122593(-;-)
Make rs398122593(-;AA)
Make rs398122593(AA;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32362607
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122593
ebirs398122593
HLIrs398122593
Exacrs398122593
Varsomers398122593
Maprs398122593
PheGenIrs398122593
hapmaprs398122593
1000 genomesrs398122593
hgdprs398122593
ensemblrs398122593
gopubmedrs398122593
geneviewrs398122593
scholarrs398122593
googlers398122593
pharmgkbrs398122593
gwascentralrs398122593
openSNPrs398122593
23andMers398122593
23andMe allrs398122593
SNP Nexus

SNPshotrs398122593
SNPdbers398122593
MSV3drs398122593
GWAS Ctlgrs398122593
Max Magnitude0
ClinVar
Risk rs398122593(AA;AA)
Alt rs398122593(AA;AA)
Reference rs398122593(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32936743_32936744dupAA
CLNSRC ClinVar
CLNACC RCV000077014.2,