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rs104894220

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894220(A;A)
Make rs104894220(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position113416935
GeneDRD2
is asnp
is mentioned by
dbSNPrs104894220
ebirs104894220
HLIrs104894220
Exacrs104894220
Varsomers104894220
Maprs104894220
PheGenIrs104894220
hapmaprs104894220
1000 genomesrs104894220
hgdprs104894220
ensemblrs104894220
gopubmedrs104894220
geneviewrs104894220
scholarrs104894220
googlers104894220
pharmgkbrs104894220
gwascentralrs104894220
openSNPrs104894220
23andMers104894220
23andMe allrs104894220
SNP Nexus

SNPshotrs104894220
SNPdbers104894220
MSV3drs104894220
GWAS Ctlgrs104894220
Max Magnitude0
OMIM126450
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894220(A;A)
Alt rs104894220(A;A)
Reference rs104894220(G;G)
Significance Pathogenic
Disease Myoclonic dystonia
Variation info
Gene DRD2
CLNDBN Myoclonic dystonia
Reversed 1
HGVS NC_000011.9:g.113287657C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018259.28,