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rs281864720

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281864720(G;G)
Make rs281864720(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position29213994
GeneALK
is asnp
is mentioned by
dbSNPrs281864720
ebirs281864720
HLIrs281864720
Exacrs281864720
Varsomers281864720
Maprs281864720
PheGenIrs281864720
hapmaprs281864720
1000 genomesrs281864720
hgdprs281864720
ensemblrs281864720
gopubmedrs281864720
geneviewrs281864720
scholarrs281864720
googlers281864720
pharmgkbrs281864720
gwascentralrs281864720
openSNPrs281864720
23andMers281864720
23andMe allrs281864720
SNP Nexus

SNPshotrs281864720
SNPdbers281864720
MSV3drs281864720
GWAS Ctlgrs281864720
Max Magnitude0
ClinVar
Risk rs281864720(G;G)
Alt rs281864720(G;G)
Reference rs281864720(T;T)
Significance Pathogenic
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29436860A>C; NC_000002.11:g.29436860A>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055895.1, RCV000201924.1,