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rs397507828

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507828(G;T)
Make rs397507828(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340440
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507828
ebirs397507828
HLIrs397507828
Exacrs397507828
Varsomers397507828
Maprs397507828
PheGenIrs397507828
hapmaprs397507828
1000 genomesrs397507828
hgdprs397507828
ensemblrs397507828
gopubmedrs397507828
geneviewrs397507828
scholarrs397507828
googlers397507828
pharmgkbrs397507828
gwascentralrs397507828
openSNPrs397507828
23andMers397507828
23andMe allrs397507828
SNP Nexus

SNPshotrs397507828
SNPdbers397507828
MSV3drs397507828
GWAS Ctlgrs397507828
Max Magnitude0
ClinVar
Risk rs397507828(T;T)
Alt rs397507828(T;T)
Reference rs397507828(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32914577G>T
CLNSRC ClinVar
CLNACC RCV000044840.2,