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rs1057520019

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520019(G;G)
Make rs1057520019(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position29222362
GeneALK
is asnp
is mentioned by
dbSNPrs1057520019
dbSNP (old)rs1057520019
ClinGenrs1057520019
ebirs1057520019
HLIrs1057520019
Exacrs1057520019
Gnomadrs1057520019
Varsomers1057520019
Maprs1057520019
PheGenIrs1057520019
Biobankrs1057520019
1000 genomesrs1057520019
hgdprs1057520019
ensemblrs1057520019
gopubmedrs1057520019
geneviewrs1057520019
scholarrs1057520019
googlers1057520019
pharmgkbrs1057520019
gwascentralrs1057520019
openSNPrs1057520019
23andMers1057520019
23andMe allrs1057520019
SNPshotrs1057520019
SNPdbers1057520019
MSV3drs1057520019
GWAS Ctlgrs1057520019
Max Magnitude0
ClinVar
Risk rs1057520019(G;G)
Alt rs1057520019(G;G)
Reference Rs1057520019(T;T)
Significance Probable-Pathogenic
Disease Neuroblastoma
Variation info
Gene ALK
CLNDBN Neuroblastoma
Reversed 1
HGVS NC_000002.11:g.29445228A>C
CLNSRC
CLNACC RCV000422585.1,