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rs398122530

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122530(-;-)
Make rs398122530(-;A)
Make rs398122530(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339698
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122530
ebirs398122530
HLIrs398122530
Exacrs398122530
Varsomers398122530
Maprs398122530
PheGenIrs398122530
hapmaprs398122530
1000 genomesrs398122530
hgdprs398122530
ensemblrs398122530
gopubmedrs398122530
geneviewrs398122530
scholarrs398122530
googlers398122530
pharmgkbrs398122530
gwascentralrs398122530
openSNPrs398122530
23andMers398122530
23andMe allrs398122530
SNP Nexus

SNPshotrs398122530
SNPdbers398122530
MSV3drs398122530
GWAS Ctlgrs398122530
Max Magnitude0
ClinVar
Risk rs398122530(A;A)
Alt rs398122530(A;A)
Reference rs398122530(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913835_32913836insA
CLNSRC ClinVar
CLNACC RCV000076929.2,