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rs397507844

From SNPedia

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


Make rs397507844(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340708
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507844
dbSNP (old)rs397507844
ClinGenrs397507844
ebirs397507844
HLIrs397507844
Exacrs397507844
Gnomadrs397507844
Varsomers397507844
Maprs397507844
PheGenIrs397507844
Biobankrs397507844
1000 genomesrs397507844
hgdprs397507844
ensemblrs397507844
gopubmedrs397507844
geneviewrs397507844
scholarrs397507844
googlers397507844
pharmgkbrs397507844
gwascentralrs397507844
openSNPrs397507844
23andMers397507844
23andMe allrs397507844
SNP Nexus

SNPshotrs397507844
SNPdbers397507844
MSV3drs397507844
GWAS Ctlgrs397507844
Max Magnitude6
ClinVar
Risk rs397507844(-;-)
Alt rs397507844(-;-)
Reference Rs397507844(TGTAAACTCAGAAA;TGTAAACTCAGAAA)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914845_32914858delTAAACTCAGAAATG
CLNSRC ClinVar
CLNACC RCV000044922.2, RCV000257701.2,