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rs113994092

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs113994092(C;C)
Make rs113994092(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position29209873
GeneALK
is asnp
is mentioned by
dbSNPrs113994092
ebirs113994092
HLIrs113994092
Exacrs113994092
Varsomers113994092
Maprs113994092
PheGenIrs113994092
hapmaprs113994092
1000 genomesrs113994092
hgdprs113994092
ensemblrs113994092
gopubmedrs113994092
geneviewrs113994092
scholarrs113994092
googlers113994092
pharmgkbrs113994092
gwascentralrs113994092
openSNPrs113994092
23andMers113994092
23andMe allrs113994092
SNP Nexus

SNPshotrs113994092
SNPdbers113994092
MSV3drs113994092
GWAS Ctlgrs113994092
Max Magnitude0
ClinVar
Risk rs113994092(C;C)
Alt rs113994092(C;C)
Reference rs113994092(T;T)
Significance Pathogenic
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29432739A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000021080.1,


OMIM613014
Desc
Variant
Relatedalso