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rs397507883

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507883(G;G)
Make rs397507883(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319068
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507883
ebirs397507883
HLIrs397507883
Exacrs397507883
Varsomers397507883
Maprs397507883
PheGenIrs397507883
hapmaprs397507883
1000 genomesrs397507883
hgdprs397507883
ensemblrs397507883
gopubmedrs397507883
geneviewrs397507883
scholarrs397507883
googlers397507883
pharmgkbrs397507883
gwascentralrs397507883
openSNPrs397507883
23andMers397507883
23andMe allrs397507883
SNP Nexus

SNPshotrs397507883
SNPdbers397507883
MSV3drs397507883
GWAS Ctlgrs397507883
Max Magnitude0
ClinVar
Risk rs397507883(G;G)
Alt rs397507883(G;G)
Reference rs397507883(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32893205T>G
CLNSRC ClinVar
CLNACC RCV000045053.2,