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rs397508026

From SNPedia

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


Make rs397508026(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379774
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397508026
ClinGenrs397508026
ebirs397508026
HLIrs397508026
Exacrs397508026
Varsomers397508026
Maprs397508026
PheGenIrs397508026
hapmaprs397508026
1000 genomesrs397508026
hgdprs397508026
ensemblrs397508026
gopubmedrs397508026
geneviewrs397508026
scholarrs397508026
googlers397508026
pharmgkbrs397508026
gwascentralrs397508026
openSNPrs397508026
23andMers397508026
23andMe allrs397508026
SNP Nexus

SNPshotrs397508026
SNPdbers397508026
MSV3drs397508026
GWAS Ctlgrs397508026
Max Magnitude6
ClinVar
Risk rs397508026(-;-)
Alt rs397508026(-;-)
Reference Rs397508026(ATCATCAGATTTAT;ATCATCAGATTTAT)
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.32953911_32953924delCATCAGATTTATAT
CLNSRC ClinVar
CLNACC RCV000045678.2, RCV000257752.2,