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rs121908449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908449(C;C)
Make rs121908449(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position65197160
GeneRGS9
is asnp
is mentioned by
dbSNPrs121908449
ebirs121908449
HLIrs121908449
Exacrs121908449
Varsomers121908449
Maprs121908449
PheGenIrs121908449
hapmaprs121908449
1000 genomesrs121908449
hgdprs121908449
ensemblrs121908449
gopubmedrs121908449
geneviewrs121908449
scholarrs121908449
googlers121908449
pharmgkbrs121908449
gwascentralrs121908449
openSNPrs121908449
23andMers121908449
23andMe allrs121908449
SNP Nexus

SNPshotrs121908449
SNPdbers121908449
MSV3drs121908449
GWAS Ctlgrs121908449
Max Magnitude0
OMIM604067
Desc
Variant0001
Relatedalso
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
CLNACC RCV000006220.2,