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rs397507804

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAG;AGAG) 0 common in clinvar
Make rs397507804(-;-)
Make rs397507804(-;AGAG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340129
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507804
ebirs397507804
HLIrs397507804
Exacrs397507804
Varsomers397507804
Maprs397507804
PheGenIrs397507804
hapmaprs397507804
1000 genomesrs397507804
hgdprs397507804
ensemblrs397507804
gopubmedrs397507804
geneviewrs397507804
scholarrs397507804
googlers397507804
pharmgkbrs397507804
gwascentralrs397507804
openSNPrs397507804
23andMers397507804
23andMe allrs397507804
SNP Nexus

SNPshotrs397507804
SNPdbers397507804
MSV3drs397507804
GWAS Ctlgrs397507804
Max Magnitude0
ClinVar
Risk rs397507804(;)
Alt rs397507804(;)
Reference rs397507804(AGAG;AGAG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914266_32914269delAGAG
CLNSRC ClinVar
CLNACC RCV000044751.2,