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rs875989841

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs875989841(C;C)
Make rs875989841(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position165418735
GenePDE10A
is asnp
is mentioned by
dbSNPrs875989841
ebirs875989841
HLIrs875989841
Exacrs875989841
Varsomers875989841
Maprs875989841
PheGenIrs875989841
hapmaprs875989841
1000 genomesrs875989841
hgdprs875989841
ensemblrs875989841
gopubmedrs875989841
geneviewrs875989841
scholarrs875989841
googlers875989841
pharmgkbrs875989841
gwascentralrs875989841
openSNPrs875989841
23andMers875989841
23andMe allrs875989841
SNP Nexus

SNPshotrs875989841
SNPdbers875989841
MSV3drs875989841
GWAS Ctlgrs875989841
Max Magnitude0
ClinVar
Risk rs875989841(C;C)
Alt rs875989841(C;C)
Reference rs875989841(T;T)
Significance Pathogenic
Disease Striatal degeneration
Variation info
Gene PDE10A
CLNDBN Striatal degeneration, autosomal dominant 2
Reversed 1
HGVS NC_000006.11:g.165832223A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000210939.1,