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rs397507827

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507827(G;T)
Make rs397507827(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340437
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507827
ebirs397507827
HLIrs397507827
Exacrs397507827
Varsomers397507827
Maprs397507827
PheGenIrs397507827
hapmaprs397507827
1000 genomesrs397507827
hgdprs397507827
ensemblrs397507827
gopubmedrs397507827
geneviewrs397507827
scholarrs397507827
googlers397507827
pharmgkbrs397507827
gwascentralrs397507827
openSNPrs397507827
23andMers397507827
23andMe allrs397507827
SNP Nexus

SNPshotrs397507827
SNPdbers397507827
MSV3drs397507827
GWAS Ctlgrs397507827
Max Magnitude0
ClinVar
Risk rs397507827(T;T)
Alt rs397507827(T;T)
Reference rs397507827(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.32914574G>T
CLNSRC ClinVar
CLNACC RCV000044838.2,