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rs11994014

From SNPedia

Orientationplus
Stabilizedplus
Make rs11994014(A;A)
Make rs11994014(A;G)
Make rs11994014(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position24944767
is asnp
is mentioned by
dbSNPrs11994014
ebirs11994014
HLIrs11994014
Exacrs11994014
Varsomers11994014
Maprs11994014
PheGenIrs11994014
hapmaprs11994014
1000 genomesrs11994014
hgdprs11994014
ensemblrs11994014
gopubmedrs11994014
geneviewrs11994014
scholarrs11994014
googlers11994014
pharmgkbrs11994014
gwascentralrs11994014
openSNPrs11994014
23andMers11994014
23andMe allrs11994014
SNP Nexus

SNPshotrs11994014
SNPdbers11994014
MSV3drs11994014
GWAS Ctlgrs11994014
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 25312269OA-icon.png] Common genetic variants in NEFL influence gene expression and neuroblastoma risk