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rs398122726

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGA;AAGA) 0 common in clinvar
Make rs398122726(-;-)
Make rs398122726(-;AAGA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332877
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122726
ebirs398122726
HLIrs398122726
Exacrs398122726
Varsomers398122726
Maprs398122726
PheGenIrs398122726
hapmaprs398122726
1000 genomesrs398122726
hgdprs398122726
ensemblrs398122726
gopubmedrs398122726
geneviewrs398122726
scholarrs398122726
googlers398122726
pharmgkbrs398122726
gwascentralrs398122726
openSNPrs398122726
23andMers398122726
23andMe allrs398122726
SNP Nexus

SNPshotrs398122726
SNPdbers398122726
MSV3drs398122726
GWAS Ctlgrs398122726
Max Magnitude0
ClinVar
Risk rs398122726(;)
Alt rs398122726(;)
Reference rs398122726(AAGA;AAGA)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32907014_32907017delAAGA
CLNSRC ClinVar
CLNACC RCV000077659.2,