rs121908449

Orientation

plus

Stabilized

plus

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

Make rs121908449(C;C)

Make rs121908449(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

65197160

Gene

RGS9

is a	snp
is	mentioned by
dbSNP	rs121908449
dbSNP (classic)	rs121908449
ClinGen	rs121908449
ebi	rs121908449
HLI	rs121908449
Exac	rs121908449
Gnomad	rs121908449
Varsome	rs121908449
LitVar	rs121908449
Map	rs121908449
PheGenI	rs121908449
Biobank	rs121908449
1000 genomes	rs121908449
hgdp	rs121908449
ensembl	rs121908449
geneview	rs121908449
scholar	rs121908449
google	rs121908449
pharmgkb	rs121908449
gwascentral	rs121908449
openSNP	rs121908449
23andMe	rs121908449
SNPshot	rs121908449
SNPdbe	rs121908449
MSV3d	rs121908449
GWAS Ctlg	rs121908449

Max Magnitude

0

OMIM	604067
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121908449(C;C)
Alt	rs121908449(C;C)
Reference	Rs121908449(T;T)
Significance	Pathogenic
Disease	Prolonged electroretinal response suppression
Variation	info
Gene	RGS9
CLNDBN	Prolonged electroretinal response suppression
Reversed	0
HGVS	NC_000017.10:g.63193278T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006220.2,