rs104894220

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs104894220(A;A)

Make rs104894220(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

113416935

Gene

DRD2

is a	snp
is	mentioned by
dbSNP	rs104894220
dbSNP (classic)	rs104894220
ClinGen	rs104894220
ebi	rs104894220
HLI	rs104894220
Exac	rs104894220
Gnomad	rs104894220
Varsome	rs104894220
LitVar	rs104894220
Map	rs104894220
PheGenI	rs104894220
Biobank	rs104894220
1000 genomes	rs104894220
hgdp	rs104894220
ensembl	rs104894220
geneview	rs104894220
scholar	rs104894220
google	rs104894220
pharmgkb	rs104894220
gwascentral	rs104894220
openSNP	rs104894220
23andMe	rs104894220
SNPshot	rs104894220
SNPdbe	rs104894220
MSV3d	rs104894220
GWAS Ctlg	rs104894220

Max Magnitude

0

OMIM	126450
Desc
Variant	0001
Related	also

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 UniProtKB (protein)
CLNACC	RCV000018259.28,