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rs398122779

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122779(A;G)
Make rs398122779(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326099
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122779
dbSNP (old)rs398122779
ClinGenrs398122779
ebirs398122779
HLIrs398122779
Exacrs398122779
Varsomers398122779
Maprs398122779
PheGenIrs398122779
Biobankrs398122779
1000 genomesrs398122779
hgdprs398122779
ensemblrs398122779
gopubmedrs398122779
geneviewrs398122779
scholarrs398122779
googlers398122779
pharmgkbrs398122779
gwascentralrs398122779
openSNPrs398122779
23andMers398122779
23andMe allrs398122779
SNP Nexus

SNPshotrs398122779
SNPdbers398122779
MSV3drs398122779
GWAS Ctlgrs398122779
Max Magnitude0
ClinVar
Risk rs398122779(G;G) rs398122779(T;T)
Alt rs398122779(G;G) rs398122779(T;T)
Reference Rs398122779(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32900236A>G; NC_000013.10:g.32900236A>T
CLNSRC ClinVar
CLNACC RCV000077725.2, RCV000160018.1, RCV000258384.1,