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rs778899140

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs778899140(C;C)
Make rs778899140(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position165450268
GenePDE10A
is asnp
is mentioned by
dbSNPrs778899140
ebirs778899140
HLIrs778899140
Exacrs778899140
Varsomers778899140
Maprs778899140
PheGenIrs778899140
hapmaprs778899140
1000 genomesrs778899140
hgdprs778899140
ensemblrs778899140
gopubmedrs778899140
geneviewrs778899140
scholarrs778899140
googlers778899140
pharmgkbrs778899140
gwascentralrs778899140
openSNPrs778899140
23andMers778899140
23andMe allrs778899140
SNP Nexus

SNPshotrs778899140
SNPdbers778899140
MSV3drs778899140
GWAS Ctlgrs778899140
Max Magnitude0
ClinVar
Risk rs778899140(C;C)
Alt rs778899140(C;C)
Reference rs778899140(T;T)
Significance Pathogenic
Disease Dyskinesia
Variation info
Gene PDE10A
CLNDBN Dyskinesia, limb and orofacial, infantile-onset
Reversed 0
HGVS NC_000006.11:g.165863756T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000210940.1,