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rs397507852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507852(-;-)
Make rs397507852(-;A)
Make rs397507852(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340775
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507852
ebirs397507852
HLIrs397507852
Exacrs397507852
Varsomers397507852
Maprs397507852
PheGenIrs397507852
hapmaprs397507852
1000 genomesrs397507852
hgdprs397507852
ensemblrs397507852
gopubmedrs397507852
geneviewrs397507852
scholarrs397507852
googlers397507852
pharmgkbrs397507852
gwascentralrs397507852
openSNPrs397507852
23andMers397507852
23andMe allrs397507852
SNP Nexus

SNPshotrs397507852
SNPdbers397507852
MSV3drs397507852
GWAS Ctlgrs397507852
Max Magnitude0
ClinVar
Risk rs397507852(A;A)
Alt rs397507852(A;A)
Reference rs397507852(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914912_32914913insA
CLNSRC ClinVar
CLNACC RCV000044941.2,