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rs398122535

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTG;AGTG) 0 common in clinvar
(GTGA;GTGA) 0 common in clinvar
Make rs398122535(-;-)
Make rs398122535(-;GTGA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339939
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122535
ebirs398122535
HLIrs398122535
Exacrs398122535
Varsomers398122535
Maprs398122535
PheGenIrs398122535
hapmaprs398122535
1000 genomesrs398122535
hgdprs398122535
ensemblrs398122535
gopubmedrs398122535
geneviewrs398122535
scholarrs398122535
googlers398122535
pharmgkbrs398122535
gwascentralrs398122535
openSNPrs398122535
23andMers398122535
23andMe allrs398122535
SNP Nexus

SNPshotrs398122535
SNPdbers398122535
MSV3drs398122535
GWAS Ctlgrs398122535
Max Magnitude0
ClinVar
Risk rs398122535(;)
Alt rs398122535(;)
Reference rs398122535(AGTG;AGTG)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914076_32914079delGTGA
CLNSRC ClinVar
CLNACC RCV000076935.2,