Have questions? Visit https://www.reddit.com/r/SNPedia

rs113994088

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs113994088(C;C)
Make rs113994088(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position29222584
GeneALK
is asnp
is mentioned by
dbSNPrs113994088
ebirs113994088
HLIrs113994088
Exacrs113994088
Varsomers113994088
Maprs113994088
PheGenIrs113994088
hapmaprs113994088
1000 genomesrs113994088
hgdprs113994088
ensemblrs113994088
gopubmedrs113994088
geneviewrs113994088
scholarrs113994088
googlers113994088
pharmgkbrs113994088
gwascentralrs113994088
openSNPrs113994088
23andMers113994088
23andMe allrs113994088
SNP Nexus

SNPshotrs113994088
SNPdbers113994088
MSV3drs113994088
GWAS Ctlgrs113994088
Max Magnitude0
OMIM105590
Desc
Variant0002
Relatedalso
ClinVar
Risk rs113994088(C;C)
Alt rs113994088(C;C)
Reference rs113994088(G;G)
Significance Other
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29445450C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019710.5,