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rs863225281

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225281(A;A)
Make rs863225281(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position29220829
GeneALK
is asnp
is mentioned by
dbSNPrs863225281
ebirs863225281
HLIrs863225281
Exacrs863225281
Varsomers863225281
Maprs863225281
PheGenIrs863225281
hapmaprs863225281
1000 genomesrs863225281
hgdprs863225281
ensemblrs863225281
gopubmedrs863225281
geneviewrs863225281
scholarrs863225281
googlers863225281
pharmgkbrs863225281
gwascentralrs863225281
openSNPrs863225281
23andMers863225281
23andMe allrs863225281
SNP Nexus

SNPshotrs863225281
SNPdbers863225281
MSV3drs863225281
GWAS Ctlgrs863225281
Max Magnitude0
ClinVar
Risk rs863225281(A,G;A,G)
Alt rs863225281(A,G;A,G)
Reference rs863225281(C;C)
Significance Pathogenic
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29443695G>C; NC_000002.11:g.29443695G>T
CLNSRC
CLNACC RCV000201904.1, RCV000201882.1,