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rs1670283

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 0 common in clinvar
Make rs1670283(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position29193706
GeneALK
is asnp
is mentioned by
dbSNPrs1670283
dbSNP (classic)rs1670283
ClinGenrs1670283
ebirs1670283
HLIrs1670283
Exacrs1670283
Gnomadrs1670283
Varsomers1670283
LitVarrs1670283
Maprs1670283
PheGenIrs1670283
Biobankrs1670283
1000 genomesrs1670283
hgdprs1670283
ensemblrs1670283
geneviewrs1670283
scholarrs1670283
googlers1670283
pharmgkbrs1670283
gwascentralrs1670283
openSNPrs1670283
23andMers1670283
SNPshotrs1670283
SNPdbers1670283
MSV3drs1670283
GWAS Ctlgrs1670283
GMAF0.006887
Max Magnitude0
? (C;C) (C;T) (T;T) 28




ClinVar
Risk Rs1670283(C;C)
Alt Rs1670283(C;C)
Reference Rs1670283(T;T)
Significance Non-pathogenic
Disease not specified Neuroblastoma Susceptibility
Variation info
Gene ALK
CLNDBN not specified Neuroblastoma Susceptibility
Reversed 0
HGVS NC_000002.11:g.29416572T>C
CLNSRC UniProtKB (protein)
CLNACC RCV000119976.4, RCV000390907.1,