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rs281864719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281864719(G;G)
Make rs281864719(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position29220831
GeneALK
is asnp
is mentioned by
dbSNPrs281864719
ebirs281864719
HLIrs281864719
Exacrs281864719
Varsomers281864719
Maprs281864719
PheGenIrs281864719
hapmaprs281864719
1000 genomesrs281864719
hgdprs281864719
ensemblrs281864719
gopubmedrs281864719
geneviewrs281864719
scholarrs281864719
googlers281864719
pharmgkbrs281864719
gwascentralrs281864719
openSNPrs281864719
23andMers281864719
23andMe allrs281864719
SNP Nexus

SNPshotrs281864719
SNPdbers281864719
MSV3drs281864719
GWAS Ctlgrs281864719
Max Magnitude0
ClinVar
Risk rs281864719(G;G)
Alt rs281864719(G;G)
Reference rs281864719(T;T)
Significance Pathogenic
Disease Neuroblastoma 3
Variation info
Gene ALK
CLNDBN Neuroblastoma 3
Reversed 1
HGVS NC_000002.11:g.29443697A>C; NC_000002.11:g.29443697A>G; NC_000002.11:g.29443697A>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055894.2, RCV000201883.1, RCV000201918.1,