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

rs397507933

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507933(-;-)
Make rs397507933(-;T)
Make rs397507933(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32357805
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507933
ebirs397507933
HLIrs397507933
Exacrs397507933
Varsomers397507933
Maprs397507933
PheGenIrs397507933
hapmaprs397507933
1000 genomesrs397507933
hgdprs397507933
ensemblrs397507933
gopubmedrs397507933
geneviewrs397507933
scholarrs397507933
googlers397507933
pharmgkbrs397507933
gwascentralrs397507933
openSNPrs397507933
23andMers397507933
23andMe allrs397507933
SNP Nexus

SNPshotrs397507933
SNPdbers397507933
MSV3drs397507933
GWAS Ctlgrs397507933
Max Magnitude0
ClinVar
Risk rs397507933(T;T)
Alt rs397507933(T;T)
Reference rs397507933(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32931942_32931943insT
CLNSRC ClinVar
CLNACC RCV000045287.2,