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rs104893793

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893793(A;A)
Make rs104893793(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position129531005
GeneRHO
is asnp
is mentioned by
dbSNPrs104893793
ebirs104893793
HLIrs104893793
Exacrs104893793
Varsomers104893793
Maprs104893793
PheGenIrs104893793
hapmaprs104893793
1000 genomesrs104893793
hgdprs104893793
ensemblrs104893793
gopubmedrs104893793
geneviewrs104893793
scholarrs104893793
googlers104893793
pharmgkbrs104893793
gwascentralrs104893793
openSNPrs104893793
23andMers104893793
23andMe allrs104893793
SNP Nexus

SNPshotrs104893793
SNPdbers104893793
MSV3drs104893793
GWAS Ctlgrs104893793
Max Magnitude0
OMIM180380
Desc
Variant0037
Relatedalso
ClinVar
Risk rs104893793(A,T;A,T)
Alt rs104893793(A,T;A,T)
Reference rs104893793(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129249848C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013924.23,