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rs397507749

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507749(-;-)
Make rs397507749(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339272
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507749
ebirs397507749
HLIrs397507749
Exacrs397507749
Varsomers397507749
Maprs397507749
PheGenIrs397507749
hapmaprs397507749
1000 genomesrs397507749
hgdprs397507749
ensemblrs397507749
gopubmedrs397507749
geneviewrs397507749
scholarrs397507749
googlers397507749
pharmgkbrs397507749
gwascentralrs397507749
openSNPrs397507749
23andMers397507749
23andMe allrs397507749
SNP Nexus

SNPshotrs397507749
SNPdbers397507749
MSV3drs397507749
GWAS Ctlgrs397507749
Max Magnitude0
ClinVar
Risk rs397507749(;)
Alt rs397507749(;)
Reference rs397507749(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913409delA
CLNSRC ClinVar
CLNACC RCV000044520.2,