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rs11037575

From SNPedia

Orientationplus
Stabilizedplus
Make rs11037575(C;C)
Make rs11037575(C;T)
Make rs11037575(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position43706780
GeneHSD17B12
is asnp
is mentioned by
dbSNPrs11037575
ebirs11037575
HLIrs11037575
Exacrs11037575
Varsomers11037575
Maprs11037575
PheGenIrs11037575
hapmaprs11037575
1000 genomesrs11037575
hgdprs11037575
ensemblrs11037575
gopubmedrs11037575
geneviewrs11037575
scholarrs11037575
googlers11037575
pharmgkbrs11037575
gwascentralrs11037575
openSNPrs11037575
23andMers11037575
23andMe allrs11037575
SNP Nexus

SNPshotrs11037575
SNPdbers11037575
MSV3drs11037575
GWAS Ctlgrs11037575
GMAF0.4527
Max Magnitude
? (C;C) (C;T) (T;T) 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 C
P-val 5E-8
Odds Ratio 1.23 [NR]


[PMID 18463370OA-icon.png] Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.


[PMID 21436895OA-icon.png] Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci.