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rs863225284

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225284(A;A)
Make rs863225284(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position29213992
GeneALK
is asnp
is mentioned by
dbSNPrs863225284
ebirs863225284
HLIrs863225284
Exacrs863225284
Varsomers863225284
Maprs863225284
PheGenIrs863225284
hapmaprs863225284
1000 genomesrs863225284
hgdprs863225284
ensemblrs863225284
gopubmedrs863225284
geneviewrs863225284
scholarrs863225284
googlers863225284
pharmgkbrs863225284
gwascentralrs863225284
openSNPrs863225284
23andMers863225284
23andMe allrs863225284
SNP Nexus

SNPshotrs863225284
SNPdbers863225284
MSV3drs863225284
GWAS Ctlgrs863225284
Max Magnitude0
ClinVar
Risk rs863225284(A;A)
Alt rs863225284(A;A)
Reference rs863225284(C;C)
Significance Pathogenic
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29436858G>T
CLNSRC
CLNACC RCV000201908.1,