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rs875989839

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989839(C;C)
Make rs875989839(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position165450242
GenePDE10A
is asnp
is mentioned by
dbSNPrs875989839
ebirs875989839
HLIrs875989839
Exacrs875989839
Varsomers875989839
Maprs875989839
PheGenIrs875989839
hapmaprs875989839
1000 genomesrs875989839
hgdprs875989839
ensemblrs875989839
gopubmedrs875989839
geneviewrs875989839
scholarrs875989839
googlers875989839
pharmgkbrs875989839
gwascentralrs875989839
openSNPrs875989839
23andMers875989839
23andMe allrs875989839
SNP Nexus

SNPshotrs875989839
SNPdbers875989839
MSV3drs875989839
GWAS Ctlgrs875989839
Max Magnitude0
ClinVar
Risk rs875989839(C;C)
Alt rs875989839(C;C)
Reference rs875989839(G;G)
Significance Pathogenic
Disease Dyskinesia
Variation info
Gene PDE10A
CLNDBN Dyskinesia, limb and orofacial, infantile-onset
Reversed 1
HGVS NC_000006.11:g.165863730C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000210942.1,