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rs397507406

From SNPedia

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


Make rs397507406(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371016
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507406
dbSNP (old)rs397507406
ClinGenrs397507406
ebirs397507406
HLIrs397507406
Exacrs397507406
Gnomadrs397507406
Varsomers397507406
Maprs397507406
PheGenIrs397507406
Biobankrs397507406
1000 genomesrs397507406
hgdprs397507406
ensemblrs397507406
gopubmedrs397507406
geneviewrs397507406
scholarrs397507406
googlers397507406
pharmgkbrs397507406
gwascentralrs397507406
openSNPrs397507406
23andMers397507406
23andMe allrs397507406
SNP Nexus

SNPshotrs397507406
SNPdbers397507406
MSV3drs397507406
GWAS Ctlgrs397507406
Max Magnitude6
ClinVar
Risk rs397507406(-;-)
Alt rs397507406(-;-)
Reference Rs397507406(AAGG;AAGG)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast not provided
Reversed 0
HGVS NC_000013.10:g.32945153_32945156delGAAG
CLNSRC ClinVar
CLNACC RCV000031750.4, RCV000045555.2, RCV000484733.1,