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rs398122605

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122605(-;-)
Make rs398122605(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370444
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122605
ebirs398122605
HLIrs398122605
Exacrs398122605
Varsomers398122605
Maprs398122605
PheGenIrs398122605
hapmaprs398122605
1000 genomesrs398122605
hgdprs398122605
ensemblrs398122605
gopubmedrs398122605
geneviewrs398122605
scholarrs398122605
googlers398122605
pharmgkbrs398122605
gwascentralrs398122605
openSNPrs398122605
23andMers398122605
23andMe allrs398122605
SNP Nexus

SNPshotrs398122605
SNPdbers398122605
MSV3drs398122605
GWAS Ctlgrs398122605
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs398122605(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32944581delC
CLNSRC ClinVar
CLNACC RCV000077027.3,