Have questions? Visit https://www.reddit.com/r/SNPedia

rs17468382

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17468382(C;C)
Make rs17468382(C;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position52734641
GeneDCC
is asnp
is mentioned by
dbSNPrs17468382
ebirs17468382
HLIrs17468382
Exacrs17468382
Varsomers17468382
Maprs17468382
PheGenIrs17468382
hapmaprs17468382
1000 genomesrs17468382
hgdprs17468382
ensemblrs17468382
gopubmedrs17468382
geneviewrs17468382
scholarrs17468382
googlers17468382
pharmgkbrs17468382
gwascentralrs17468382
openSNPrs17468382
23andMers17468382
23andMe allrs17468382
SNP Nexus

SNPshotrs17468382
SNPdbers17468382
MSV3drs17468382
GWAS Ctlgrs17468382
GMAF0.02663
Max Magnitude0

[PMID 21085126] SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population

[PMID 18628988OA-icon.png] Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease.