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rs104893792

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893792(C;C)
Make rs104893792(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129528884
GeneRHO
is asnp
is mentioned by
dbSNPrs104893792
ebirs104893792
HLIrs104893792
Exacrs104893792
Varsomers104893792
Maprs104893792
PheGenIrs104893792
hapmaprs104893792
1000 genomesrs104893792
hgdprs104893792
ensemblrs104893792
gopubmedrs104893792
geneviewrs104893792
scholarrs104893792
googlers104893792
pharmgkbrs104893792
gwascentralrs104893792
openSNPrs104893792
23andMers104893792
23andMe allrs104893792
SNP Nexus

SNPshotrs104893792
SNPdbers104893792
MSV3drs104893792
GWAS Ctlgrs104893792
Max Magnitude0
OMIM180380
Desc
Variant0034
Relatedalso
ClinVar
Risk rs104893792(C;C)
Alt rs104893792(C;C)
Reference rs104893792(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129247727G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013922.23,