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rs104893788

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893788(A;A)
Make rs104893788(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129529074
GeneRHO
is asnp
is mentioned by
dbSNPrs104893788
ebirs104893788
HLIrs104893788
Exacrs104893788
Varsomers104893788
Maprs104893788
PheGenIrs104893788
hapmaprs104893788
1000 genomesrs104893788
hgdprs104893788
ensemblrs104893788
gopubmedrs104893788
geneviewrs104893788
scholarrs104893788
googlers104893788
pharmgkbrs104893788
gwascentralrs104893788
openSNPrs104893788
23andMers104893788
23andMe allrs104893788
SNP Nexus

SNPshotrs104893788
SNPdbers104893788
MSV3drs104893788
GWAS Ctlgrs104893788
Max Magnitude0
OMIM180380
Desc
Variant0036
Relatedalso
ClinVar
Risk rs104893788(A,C;A,C)
Alt rs104893788(A,C;A,C)
Reference rs104893788(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129247917G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013923.24,