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rs397507861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAG;CAG) 0 common in clinvar
Make rs397507861(CAG;GACT)
Make rs397507861(GACT;GACT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340845
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507861
ebirs397507861
HLIrs397507861
Exacrs397507861
Varsomers397507861
Maprs397507861
PheGenIrs397507861
hapmaprs397507861
1000 genomesrs397507861
hgdprs397507861
ensemblrs397507861
gopubmedrs397507861
geneviewrs397507861
scholarrs397507861
googlers397507861
pharmgkbrs397507861
gwascentralrs397507861
openSNPrs397507861
23andMers397507861
23andMe allrs397507861
SNP Nexus

SNPshotrs397507861
SNPdbers397507861
MSV3drs397507861
GWAS Ctlgrs397507861
Max Magnitude0
ClinVar
Risk rs397507861(GACT;GACT)
Alt rs397507861(GACT;GACT)
Reference rs397507861(CAG;CAG)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914982_32914984delCAGinsGACT
CLNSRC ClinVar
CLNACC RCV000044969.2,