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rs397507369

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;GAGAA) 6 BRCA2 variant considered pathogenic for breast cancer
(AAGAG;AAGAG) 0 common in clinvar
(GAGAA;GAGAA) 0 common in clinvar


Make rs397507369(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340688
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507369
dbSNP (old)rs397507369
ClinGenrs397507369
ebirs397507369
HLIrs397507369
Exacrs397507369
Gnomadrs397507369
Varsomers397507369
Maprs397507369
PheGenIrs397507369
Biobankrs397507369
1000 genomesrs397507369
hgdprs397507369
ensemblrs397507369
gopubmedrs397507369
geneviewrs397507369
scholarrs397507369
googlers397507369
pharmgkbrs397507369
gwascentralrs397507369
openSNPrs397507369
23andMers397507369
23andMe allrs397507369
SNP Nexus

SNPshotrs397507369
SNPdbers397507369
MSV3drs397507369
GWAS Ctlgrs397507369
Max Magnitude6
ClinVar
Risk rs397507369(-;-)
Alt rs397507369(-;-)
Reference Rs397507369(AAGAG;AAGAG)
Significance Pathogenic
Disease Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32914825_32914829delGAGAA
CLNSRC ClinVar
CLNACC RCV000031620.4, RCV000213663.2,