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rs104893787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893787(A;A)
Make rs104893787(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129529062
GeneRHO
is asnp
is mentioned by
dbSNPrs104893787
ebirs104893787
HLIrs104893787
Exacrs104893787
Varsomers104893787
Maprs104893787
PheGenIrs104893787
hapmaprs104893787
1000 genomesrs104893787
hgdprs104893787
ensemblrs104893787
gopubmedrs104893787
geneviewrs104893787
scholarrs104893787
googlers104893787
pharmgkbrs104893787
gwascentralrs104893787
openSNPrs104893787
23andMers104893787
23andMe allrs104893787
SNP Nexus

SNPshotrs104893787
SNPdbers104893787
MSV3drs104893787
GWAS Ctlgrs104893787
Max Magnitude0
OMIM180380
Desc
Variant0035
Relatedalso
ClinVar
Risk rs104893787(A;A)
Alt rs104893787(A;A)
Reference rs104893787(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129247905G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013910.24,