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rs397507973

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507973(-;-)
Make rs397507973(-;AC)
Make rs397507973(AC;AC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363501
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507973
ebirs397507973
HLIrs397507973
Exacrs397507973
Varsomers397507973
Maprs397507973
PheGenIrs397507973
hapmaprs397507973
1000 genomesrs397507973
hgdprs397507973
ensemblrs397507973
gopubmedrs397507973
geneviewrs397507973
scholarrs397507973
googlers397507973
pharmgkbrs397507973
gwascentralrs397507973
openSNPrs397507973
23andMers397507973
23andMe allrs397507973
SNP Nexus

SNPshotrs397507973
SNPdbers397507973
MSV3drs397507973
GWAS Ctlgrs397507973
Max Magnitude0
ClinVar
Risk rs397507973(AC;AC)
Alt rs397507973(AC;AC)
Reference rs397507973(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937637_32937638dupAC
CLNSRC ClinVar
CLNACC RCV000045467.2,