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rs397507951

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507951(-;-)
Make rs397507951(-;AGAAGAT)
Make rs397507951(AGAAGAT;AGAAGAT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363210
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507951
ebirs397507951
HLIrs397507951
Exacrs397507951
Varsomers397507951
Maprs397507951
PheGenIrs397507951
hapmaprs397507951
1000 genomesrs397507951
hgdprs397507951
ensemblrs397507951
gopubmedrs397507951
geneviewrs397507951
scholarrs397507951
googlers397507951
pharmgkbrs397507951
gwascentralrs397507951
openSNPrs397507951
23andMers397507951
23andMe allrs397507951
SNP Nexus

SNPshotrs397507951
SNPdbers397507951
MSV3drs397507951
GWAS Ctlgrs397507951
Max Magnitude0
ClinVar
Risk rs397507951(AGAAGAT;AGAAGAT)
Alt rs397507951(AGAAGAT;AGAAGAT)
Reference rs397507951(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937341_32937347dupAGAAGAT
CLNSRC ClinVar
CLNACC RCV000045383.2,