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rs397507759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAATA;AAATA) 0 common in clinvar
Make rs397507759(-;-)
Make rs397507759(-;AAATA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339470
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507759
ebirs397507759
HLIrs397507759
Exacrs397507759
Varsomers397507759
Maprs397507759
PheGenIrs397507759
hapmaprs397507759
1000 genomesrs397507759
hgdprs397507759
ensemblrs397507759
gopubmedrs397507759
geneviewrs397507759
scholarrs397507759
googlers397507759
pharmgkbrs397507759
gwascentralrs397507759
openSNPrs397507759
23andMers397507759
23andMe allrs397507759
SNP Nexus

SNPshotrs397507759
SNPdbers397507759
MSV3drs397507759
GWAS Ctlgrs397507759
Max Magnitude0
ClinVar
Risk rs397507759(;)
Alt rs397507759(;)
Reference rs397507759(AAATA;AAATA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913607_32913611delAAATA
CLNSRC ClinVar
CLNACC RCV000044560.2,