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rs397507758

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507758(C;T)
Make rs397507758(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339456
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507758
ebirs397507758
HLIrs397507758
Exacrs397507758
Varsomers397507758
Maprs397507758
PheGenIrs397507758
hapmaprs397507758
1000 genomesrs397507758
hgdprs397507758
ensemblrs397507758
gopubmedrs397507758
geneviewrs397507758
scholarrs397507758
googlers397507758
pharmgkbrs397507758
gwascentralrs397507758
openSNPrs397507758
23andMers397507758
23andMe allrs397507758
SNP Nexus

SNPshotrs397507758
SNPdbers397507758
MSV3drs397507758
GWAS Ctlgrs397507758
Max Magnitude0
ClinVar
Risk rs397507758(T;T)
Alt rs397507758(T;T)
Reference rs397507758(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913593C>T
CLNSRC ClinVar
CLNACC RCV000044555.2,