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rs875989788

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989788(A;A)
Make rs875989788(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position100539839
GeneGPR88
is asnp
is mentioned by
dbSNPrs875989788
ebirs875989788
HLIrs875989788
Exacrs875989788
Varsomers875989788
Maprs875989788
PheGenIrs875989788
hapmaprs875989788
1000 genomesrs875989788
hgdprs875989788
ensemblrs875989788
gopubmedrs875989788
geneviewrs875989788
scholarrs875989788
googlers875989788
pharmgkbrs875989788
gwascentralrs875989788
openSNPrs875989788
23andMers875989788
23andMe allrs875989788
SNP Nexus

SNPshotrs875989788
SNPdbers875989788
MSV3drs875989788
GWAS Ctlgrs875989788
Max Magnitude0
ClinVar
Risk rs875989788(A;A)
Alt rs875989788(A;A)
Reference rs875989788(C;C)
Significance Pathogenic
Disease Chorea
Variation info
Gene GPR88
CLNDBN Chorea, childhood-onset, with psychomotor retardation
Reversed 0
HGVS NC_000001.10:g.101005395C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000211058.2,