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rs1901650

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs1901650(A;A)
Make rs1901650(A;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position14822888
GeneCDNF
is asnp
is mentioned by
dbSNPrs1901650
ebirs1901650
HLIrs1901650
Exacrs1901650
Varsomers1901650
Maprs1901650
PheGenIrs1901650
hapmaprs1901650
1000 genomesrs1901650
hgdprs1901650
ensemblrs1901650
gopubmedrs1901650
geneviewrs1901650
scholarrs1901650
googlers1901650
pharmgkbrs1901650
gwascentralrs1901650
openSNPrs1901650
23andMers1901650
23andMe allrs1901650
SNP Nexus

SNPshotrs1901650
SNPdbers1901650
MSV3drs1901650
GWAS Ctlgrs1901650
GMAF0.03535
Max Magnitude0
? (A;A) (A;T) (T;T) 28

[PMID 21320571] Analysis of mutations and the association between polymorphisms in the cerebral dopamine neurotrophic factor (CDNF) gene and Parkinson disease