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rs397507825

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACAT;ACAT) 0 common in clinvar
Make rs397507825(-;-)
Make rs397507825(-;ACAT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340415
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507825
ebirs397507825
HLIrs397507825
Exacrs397507825
Varsomers397507825
Maprs397507825
PheGenIrs397507825
hapmaprs397507825
1000 genomesrs397507825
hgdprs397507825
ensemblrs397507825
gopubmedrs397507825
geneviewrs397507825
scholarrs397507825
googlers397507825
pharmgkbrs397507825
gwascentralrs397507825
openSNPrs397507825
23andMers397507825
23andMe allrs397507825
SNP Nexus

SNPshotrs397507825
SNPdbers397507825
MSV3drs397507825
GWAS Ctlgrs397507825
Max Magnitude0
ClinVar
Risk rs397507825(;)
Alt rs397507825(;)
Reference rs397507825(ACAT;ACAT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914552_32914555delACAT
CLNSRC ClinVar
CLNACC RCV000044829.2,