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rs113994090

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113994090(C;T)
Make rs113994090(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position29223441
GeneALK
is asnp
is mentioned by
dbSNPrs113994090
ClinGenrs113994090
ebirs113994090
HLIrs113994090
Exacrs113994090
Varsomers113994090
Maprs113994090
PheGenIrs113994090
hapmaprs113994090
1000 genomesrs113994090
hgdprs113994090
ensemblrs113994090
gopubmedrs113994090
geneviewrs113994090
scholarrs113994090
googlers113994090
pharmgkbrs113994090
gwascentralrs113994090
openSNPrs113994090
23andMers113994090
23andMe allrs113994090
SNP Nexus

SNPshotrs113994090
SNPdbers113994090
MSV3drs113994090
GWAS Ctlgrs113994090
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs113994090(T;T)
Alt rs113994090(T;T)
Reference Rs113994090(C;C)
Significance Other
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29446307G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020581.1,


OMIM613014
Desc
Variant
Relatedalso