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rs104893774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893774(G;T)
Make rs104893774(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position129530918
GeneRHO
is asnp
is mentioned by
dbSNPrs104893774
ebirs104893774
HLIrs104893774
Exacrs104893774
Varsomers104893774
Maprs104893774
PheGenIrs104893774
hapmaprs104893774
1000 genomesrs104893774
hgdprs104893774
ensemblrs104893774
gopubmedrs104893774
geneviewrs104893774
scholarrs104893774
googlers104893774
pharmgkbrs104893774
gwascentralrs104893774
openSNPrs104893774
23andMers104893774
23andMe allrs104893774
SNP Nexus

SNPshotrs104893774
SNPdbers104893774
MSV3drs104893774
GWAS Ctlgrs104893774
Max Magnitude0
OMIM180380
Desc
Variant0011
Relatedalso
ClinVar
Risk rs104893774(A,T;A,T)
Alt rs104893774(A,T;A,T)
Reference rs104893774(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129249761G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013898.24,