Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507934

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507934(-;-)
Make rs397507934(-;A)
Make rs397507934(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357821
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507934
ebirs397507934
HLIrs397507934
Exacrs397507934
Varsomers397507934
Maprs397507934
PheGenIrs397507934
hapmaprs397507934
1000 genomesrs397507934
hgdprs397507934
ensemblrs397507934
gopubmedrs397507934
geneviewrs397507934
scholarrs397507934
googlers397507934
pharmgkbrs397507934
gwascentralrs397507934
openSNPrs397507934
23andMers397507934
23andMe allrs397507934
SNP Nexus

SNPshotrs397507934
SNPdbers397507934
MSV3drs397507934
GWAS Ctlgrs397507934
Max Magnitude0
ClinVar
Risk rs397507934(A;A)
Alt rs397507934(A;A)
Reference rs397507934(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32931958dupA
CLNSRC ClinVar
CLNACC RCV000045291.2,