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rs113994091

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs113994091(C;T)
Make rs113994091(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position29222407
GeneALK
is asnp
is mentioned by
dbSNPrs113994091
ebirs113994091
HLIrs113994091
Exacrs113994091
Varsomers113994091
Maprs113994091
PheGenIrs113994091
hapmaprs113994091
1000 genomesrs113994091
hgdprs113994091
ensemblrs113994091
gopubmedrs113994091
geneviewrs113994091
scholarrs113994091
googlers113994091
pharmgkbrs113994091
gwascentralrs113994091
openSNPrs113994091
23andMers113994091
23andMe allrs113994091
SNP Nexus

SNPshotrs113994091
SNPdbers113994091
MSV3drs113994091
GWAS Ctlgrs113994091
Max Magnitude0
OMIM105590
Desc
Variant0004
Relatedalso
ClinVar
Risk rs113994091(G,T;G,T)
Alt rs113994091(G,T;G,T)
Reference rs113994091(C;C)
Significance Other
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29445273G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019712.4,