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rs863225283

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225283(G;G)
Make rs863225283(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position29213993
GeneALK
is asnp
is mentioned by
dbSNPrs863225283
ebirs863225283
HLIrs863225283
Exacrs863225283
Varsomers863225283
Maprs863225283
PheGenIrs863225283
hapmaprs863225283
1000 genomesrs863225283
hgdprs863225283
ensemblrs863225283
gopubmedrs863225283
geneviewrs863225283
scholarrs863225283
googlers863225283
pharmgkbrs863225283
gwascentralrs863225283
openSNPrs863225283
23andMers863225283
23andMe allrs863225283
SNP Nexus

SNPshotrs863225283
SNPdbers863225283
MSV3drs863225283
GWAS Ctlgrs863225283
Max Magnitude0
ClinVar
Risk rs863225283(G;G)
Alt rs863225283(G;G)
Reference rs863225283(T;T)
Significance Pathogenic
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29436859A>C
CLNSRC
CLNACC RCV000201887.1,