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rs863225282

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225282(G;G)
Make rs863225282(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position29214009
GeneALK
is asnp
is mentioned by
dbSNPrs863225282
ebirs863225282
HLIrs863225282
Exacrs863225282
Varsomers863225282
Maprs863225282
PheGenIrs863225282
hapmaprs863225282
1000 genomesrs863225282
hgdprs863225282
ensemblrs863225282
gopubmedrs863225282
geneviewrs863225282
scholarrs863225282
googlers863225282
pharmgkbrs863225282
gwascentralrs863225282
openSNPrs863225282
23andMers863225282
23andMe allrs863225282
SNP Nexus

SNPshotrs863225282
SNPdbers863225282
MSV3drs863225282
GWAS Ctlgrs863225282
Max Magnitude0
ClinVar
Risk rs863225282(G;G)
Alt rs863225282(G;G)
Reference rs863225282(T;T)
Significance Probable-Pathogenic
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29436875A>C
CLNSRC
CLNACC RCV000201906.1,