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rs397507362

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGATAG;AAGATAG) 0 common in clinvar
(ATAGAAG;ATAGAAG) 0 common in clinvar
Make rs397507362(-;-)
Make rs397507362(-;AAGATAG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340366
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507362
ebirs397507362
HLIrs397507362
Exacrs397507362
Varsomers397507362
Maprs397507362
PheGenIrs397507362
hapmaprs397507362
1000 genomesrs397507362
hgdprs397507362
ensemblrs397507362
gopubmedrs397507362
geneviewrs397507362
scholarrs397507362
googlers397507362
pharmgkbrs397507362
gwascentralrs397507362
openSNPrs397507362
23andMers397507362
23andMe allrs397507362
SNP Nexus

SNPshotrs397507362
SNPdbers397507362
MSV3drs397507362
GWAS Ctlgrs397507362
Max Magnitude0
ClinVar
Risk rs397507362(;)
Alt rs397507362(;)
Reference rs397507362(ATAGAAG;ATAGAAG)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914503_32914509delAAGATAG
CLNSRC ClinVar
CLNACC RCV000031594.3,