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rs104893773

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893773(G;T)
Make rs104893773(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position129529049
GeneRHO
is asnp
is mentioned by
dbSNPrs104893773
ebirs104893773
HLIrs104893773
Exacrs104893773
Varsomers104893773
Maprs104893773
PheGenIrs104893773
hapmaprs104893773
1000 genomesrs104893773
hgdprs104893773
ensemblrs104893773
gopubmedrs104893773
geneviewrs104893773
scholarrs104893773
googlers104893773
pharmgkbrs104893773
gwascentralrs104893773
openSNPrs104893773
23andMers104893773
23andMe allrs104893773
SNP Nexus

SNPshotrs104893773
SNPdbers104893773
MSV3drs104893773
GWAS Ctlgrs104893773
Merged fromRs28933994
Max Magnitude0
OMIM180380
Desc
Variant0025
Relatedalso
OMIM180380
Desc
Variant0010
Relatedalso
ClinVar
Risk rs104893773(A,T;A,T)
Alt rs104893773(A,T;A,T)
Reference rs104893773(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129247892G>A; NC_000003.11:g.129247892G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013913.24, RCV000013896.23,