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rs587776710

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776710(-;-)
Make rs587776710(-;GGG)
Make rs587776710(GGG;GGG)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position11890994
GeneETV6
is asnp
is mentioned by
dbSNPrs587776710
ebirs587776710
HLIrs587776710
Exacrs587776710
Varsomers587776710
Maprs587776710
PheGenIrs587776710
hapmaprs587776710
1000 genomesrs587776710
hgdprs587776710
ensemblrs587776710
gopubmedrs587776710
geneviewrs587776710
scholarrs587776710
googlers587776710
pharmgkbrs587776710
gwascentralrs587776710
openSNPrs587776710
23andMers587776710
23andMe allrs587776710
SNP Nexus

SNPshotrs587776710
SNPdbers587776710
MSV3drs587776710
GWAS Ctlgrs587776710
Max Magnitude0
ClinVar
Risk rs587776710(GGG;GGG)
Alt rs587776710(GGG;GGG)
Reference rs587776710(;)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene ETV6
CLNDBN Acute myeloid leukemia
Reversed 0
HGVS NC_000012.11:g.12043928_12043929insGGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000009548.4,