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rs113994089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs113994089(C;C)
Make rs113994089(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position29220776
GeneALK
is asnp
is mentioned by
dbSNPrs113994089
ebirs113994089
HLIrs113994089
Exacrs113994089
Varsomers113994089
Maprs113994089
PheGenIrs113994089
hapmaprs113994089
1000 genomesrs113994089
hgdprs113994089
ensemblrs113994089
gopubmedrs113994089
geneviewrs113994089
scholarrs113994089
googlers113994089
pharmgkbrs113994089
gwascentralrs113994089
openSNPrs113994089
23andMers113994089
23andMe allrs113994089
SNP Nexus

SNPshotrs113994089
SNPdbers113994089
MSV3drs113994089
GWAS Ctlgrs113994089
Max Magnitude0
OMIM105590
Desc
Variant0003
Relatedalso
ClinVar
Risk rs113994089(C;C)
Alt rs113994089(C;C)
Reference rs113994089(G;G)
Significance Other
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29443642C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019711.5,