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rs104893797

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893797(C;G)
Make rs104893797(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129528800
GeneRHO
is asnp
is mentioned by
dbSNPrs104893797
ebirs104893797
HLIrs104893797
Exacrs104893797
Varsomers104893797
Maprs104893797
PheGenIrs104893797
hapmaprs104893797
1000 genomesrs104893797
hgdprs104893797
ensemblrs104893797
gopubmedrs104893797
geneviewrs104893797
scholarrs104893797
googlers104893797
pharmgkbrs104893797
gwascentralrs104893797
openSNPrs104893797
23andMers104893797
23andMe allrs104893797
SNP Nexus

SNPshotrs104893797
SNPdbers104893797
MSV3drs104893797
GWAS Ctlgrs104893797
Max Magnitude0
OMIM180380
Desc
Variant0043
Relatedalso
ClinVar
Risk rs104893797(G;G)
Alt rs104893797(G;G)
Reference rs104893797(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129247643C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013930.24,