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rs398122609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122609(-;-)
Make rs398122609(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379856
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122609
ebirs398122609
HLIrs398122609
Exacrs398122609
Varsomers398122609
Maprs398122609
PheGenIrs398122609
hapmaprs398122609
1000 genomesrs398122609
hgdprs398122609
ensemblrs398122609
gopubmedrs398122609
geneviewrs398122609
scholarrs398122609
googlers398122609
pharmgkbrs398122609
gwascentralrs398122609
openSNPrs398122609
23andMers398122609
23andMe allrs398122609
SNP Nexus

SNPshotrs398122609
SNPdbers398122609
MSV3drs398122609
GWAS Ctlgrs398122609
Max Magnitude0
ClinVar
Risk rs398122609(;)
Alt rs398122609(;)
Reference rs398122609(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32953993delT
CLNSRC ClinVar
CLNACC RCV000077033.2,