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rs17065417

From SNPedia

Orientationplus
Stabilizedplus
Make rs17065417(A;A)
Make rs17065417(A;C)
Make rs17065417(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position104958399
GeneLIN28B
is asnp
is mentioned by
dbSNPrs17065417
ebirs17065417
HLIrs17065417
Exacrs17065417
Varsomers17065417
Maprs17065417
PheGenIrs17065417
hapmaprs17065417
1000 genomesrs17065417
hgdprs17065417
ensemblrs17065417
gopubmedrs17065417
geneviewrs17065417
scholarrs17065417
googlers17065417
pharmgkbrs17065417
gwascentralrs17065417
openSNPrs17065417
23andMers17065417
23andMe allrs17065417
SNP Nexus

SNPshotrs17065417
SNPdbers17065417
MSV3drs17065417
GWAS Ctlgrs17065417
GMAF0.06428
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22941191OA-icon.png]
Trait Neuroblastoma
Title Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.
Risk Allele A
P-val 1E-8
Odds Ratio 1.38 [1.23-1.54]