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rs10788972

From SNPedia

Orientationplus
Make rs10788972(A;A)
Make rs10788972(A;C)
Make rs10788972(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position54106570
GeneTCEANC2
is asnp
is mentioned by
dbSNPrs10788972
ebirs10788972
HLIrs10788972
Exacrs10788972
Varsomers10788972
Maprs10788972
PheGenIrs10788972
hapmaprs10788972
1000 genomesrs10788972
hgdprs10788972
ensemblrs10788972
gopubmedrs10788972
geneviewrs10788972
scholarrs10788972
googlers10788972
pharmgkbrs10788972
gwascentralrs10788972
openSNPrs10788972
23andMers10788972
23andMe allrs10788972
SNP Nexus

SNPshotrs10788972
SNPdbers10788972
MSV3drs10788972
GWAS Ctlgrs10788972
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 26432391] TCEANC2 rs10788972 and rs12046178 variants in the PARK10 region in Chinese Han patients with sporadic Parkinson's disease