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rs397508043

From SNPedia

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


Make rs397508043(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394707
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508043
dbSNP (old)rs397508043
ClinGenrs397508043
ebirs397508043
HLIrs397508043
Exacrs397508043
Gnomadrs397508043
Varsomers397508043
Maprs397508043
PheGenIrs397508043
Biobankrs397508043
1000 genomesrs397508043
hgdprs397508043
ensemblrs397508043
gopubmedrs397508043
geneviewrs397508043
scholarrs397508043
googlers397508043
pharmgkbrs397508043
gwascentralrs397508043
openSNPrs397508043
23andMers397508043
23andMe allrs397508043
SNP Nexus

SNPshotrs397508043
SNPdbers397508043
MSV3drs397508043
GWAS Ctlgrs397508043
Max Magnitude6
ClinVar
Risk rs397508043(-;-)
Alt rs397508043(-;-)
Reference Rs397508043(TA;TA)
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.32968844_32968845delAT
CLNSRC ClinVar
CLNACC RCV000045775.2, RCV000257174.2,