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rs397507744

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507744(-;-)
Make rs397507744(-;G)
Make rs397507744(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339183
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507744
ebirs397507744
HLIrs397507744
Exacrs397507744
Varsomers397507744
Maprs397507744
PheGenIrs397507744
hapmaprs397507744
1000 genomesrs397507744
hgdprs397507744
ensemblrs397507744
gopubmedrs397507744
geneviewrs397507744
scholarrs397507744
googlers397507744
pharmgkbrs397507744
gwascentralrs397507744
openSNPrs397507744
23andMers397507744
23andMe allrs397507744
SNP Nexus

SNPshotrs397507744
SNPdbers397507744
MSV3drs397507744
GWAS Ctlgrs397507744
Max Magnitude0
ClinVar
Risk rs397507744(G;G)
Alt rs397507744(G;G)
Reference rs397507744(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913320dupG
CLNSRC ClinVar
CLNACC RCV000044499.2,