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rs875989840

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs875989840(C;C)
Make rs875989840(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position165416280
GenePDE10A
is asnp
is mentioned by
dbSNPrs875989840
ebirs875989840
HLIrs875989840
Exacrs875989840
Varsomers875989840
Maprs875989840
PheGenIrs875989840
hapmaprs875989840
1000 genomesrs875989840
hgdprs875989840
ensemblrs875989840
gopubmedrs875989840
geneviewrs875989840
scholarrs875989840
googlers875989840
pharmgkbrs875989840
gwascentralrs875989840
openSNPrs875989840
23andMers875989840
23andMe allrs875989840
SNP Nexus

SNPshotrs875989840
SNPdbers875989840
MSV3drs875989840
GWAS Ctlgrs875989840
Max Magnitude0
ClinVar
Risk rs875989840(C;C)
Alt rs875989840(C;C)
Reference rs875989840(T;T)
Significance Pathogenic
Disease Striatal degeneration
Variation info
Gene PDE10A
CLNDBN Striatal degeneration, autosomal dominant 2
Reversed 1
HGVS NC_000006.11:g.165829768A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000210938.1,