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

rs397507652

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507652(A;T)
Make rs397507652(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337398
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507652
ebirs397507652
HLIrs397507652
Exacrs397507652
Varsomers397507652
Maprs397507652
PheGenIrs397507652
hapmaprs397507652
1000 genomesrs397507652
hgdprs397507652
ensemblrs397507652
gopubmedrs397507652
geneviewrs397507652
scholarrs397507652
googlers397507652
pharmgkbrs397507652
gwascentralrs397507652
openSNPrs397507652
23andMers397507652
23andMe allrs397507652
SNP Nexus

SNPshotrs397507652
SNPdbers397507652
MSV3drs397507652
GWAS Ctlgrs397507652
Max Magnitude0
ClinVar
Risk rs397507652(T;T)
Alt rs397507652(T;T)
Reference rs397507652(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911535A>T
CLNSRC ClinVar
CLNACC RCV000044106.2,