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rs121434562

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434562(A;A)
Make rs121434562(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position41101297
GeneTAMM41, TOP1
is asnp
is mentioned by
dbSNPrs121434562
ebirs121434562
HLIrs121434562
Exacrs121434562
Varsomers121434562
Maprs121434562
PheGenIrs121434562
hapmaprs121434562
1000 genomesrs121434562
hgdprs121434562
ensemblrs121434562
gopubmedrs121434562
geneviewrs121434562
scholarrs121434562
googlers121434562
pharmgkbrs121434562
gwascentralrs121434562
openSNPrs121434562
23andMers121434562
23andMe allrs121434562
SNP Nexus

SNPshotrs121434562
SNPdbers121434562
MSV3drs121434562
GWAS Ctlgrs121434562
Max Magnitude0
OMIM126420
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434562(A;A)
Alt rs121434562(A;A)
Reference rs121434562(G;G)
Significance Pathogenic
Disease DNA topoisomerase I
Variation info
Gene TOP1 LOC101927117 PLCG1-AS1
CLNDBN DNA topoisomerase I, camptothecin-resistant
Reversed 0
HGVS NC_000020.10:g.39729937G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018262.23,