rs875989788

Orientation

plus

Stabilized

plus

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

Make rs875989788(A;A)

Make rs875989788(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

100539839

Gene

GPR88

is a	snp
is	mentioned by
dbSNP	rs875989788
dbSNP (classic)	rs875989788
ClinGen	rs875989788
ebi	rs875989788
HLI	rs875989788
Exac	rs875989788
Gnomad	rs875989788
Varsome	rs875989788
LitVar	rs875989788
Map	rs875989788
PheGenI	rs875989788
Biobank	rs875989788
1000 genomes	rs875989788
hgdp	rs875989788
ensembl	rs875989788
geneview	rs875989788
scholar	rs875989788
google	rs875989788
pharmgkb	rs875989788
gwascentral	rs875989788
openSNP	rs875989788
23andMe	rs875989788
SNPshot	rs875989788
SNPdbe	rs875989788
MSV3d	rs875989788
GWAS Ctlg	rs875989788

Max Magnitude

0

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,