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rs121434637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434637(G;T)
Make rs121434637(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position11839202
GeneETV6
is asnp
is mentioned by
dbSNPrs121434637
ebirs121434637
HLIrs121434637
Exacrs121434637
Varsomers121434637
Maprs121434637
PheGenIrs121434637
hapmaprs121434637
1000 genomesrs121434637
hgdprs121434637
ensemblrs121434637
gopubmedrs121434637
geneviewrs121434637
scholarrs121434637
googlers121434637
pharmgkbrs121434637
gwascentralrs121434637
openSNPrs121434637
23andMers121434637
23andMe allrs121434637
SNP Nexus

SNPshotrs121434637
SNPdbers121434637
MSV3drs121434637
GWAS Ctlgrs121434637
Max Magnitude0
OMIM600618
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434637(T;T)
Alt rs121434637(T;T)
Reference rs121434637(G;G)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene ETV6
CLNDBN Acute myeloid leukemia
Reversed 0
HGVS NC_000012.11:g.11992136G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009547.4,