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rs104893783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893783(G;T)
Make rs104893783(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position129532581
GeneRHO
is asnp
is mentioned by
dbSNPrs104893783
ebirs104893783
HLIrs104893783
Exacrs104893783
Varsomers104893783
Maprs104893783
PheGenIrs104893783
hapmaprs104893783
1000 genomesrs104893783
hgdprs104893783
ensemblrs104893783
gopubmedrs104893783
geneviewrs104893783
scholarrs104893783
googlers104893783
pharmgkbrs104893783
gwascentralrs104893783
openSNPrs104893783
23andMers104893783
23andMe allrs104893783
SNP Nexus

SNPshotrs104893783
SNPdbers104893783
MSV3drs104893783
GWAS Ctlgrs104893783
Max Magnitude0
OMIM180380
Desc
Variant0023
Relatedalso
ClinVar
Risk rs104893783(T;T)
Alt rs104893783(T;T)
Reference rs104893783(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4, autosomal recessive
Reversed 0
HGVS NC_000003.11:g.129251424G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013911.24,