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rs104893782

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893782(G;G)
Make rs104893782(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position129532340
GeneRHO
is asnp
is mentioned by
dbSNPrs104893782
ebirs104893782
HLIrs104893782
Exacrs104893782
Varsomers104893782
Maprs104893782
PheGenIrs104893782
hapmaprs104893782
1000 genomesrs104893782
hgdprs104893782
ensemblrs104893782
gopubmedrs104893782
geneviewrs104893782
scholarrs104893782
googlers104893782
pharmgkbrs104893782
gwascentralrs104893782
openSNPrs104893782
23andMers104893782
23andMe allrs104893782
SNP Nexus

SNPshotrs104893782
SNPdbers104893782
MSV3drs104893782
GWAS Ctlgrs104893782
Merged fromRs28933995
Max Magnitude0
OMIM180380
Desc
Variant0030
Relatedalso
OMIM180380
Desc
Variant0028
Relatedalso
ClinVar
Risk rs104893782(G;G)
Alt rs104893782(G;G)
Reference rs104893782(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129251183T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013918.23,