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rs104893778

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893778(C;T)
Make rs104893778(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position129533701
GeneRHO
is asnp
is mentioned by
dbSNPrs104893778
ebirs104893778
HLIrs104893778
Exacrs104893778
Varsomers104893778
Maprs104893778
PheGenIrs104893778
hapmaprs104893778
1000 genomesrs104893778
hgdprs104893778
ensemblrs104893778
gopubmedrs104893778
geneviewrs104893778
scholarrs104893778
googlers104893778
pharmgkbrs104893778
gwascentralrs104893778
openSNPrs104893778
23andMers104893778
23andMe allrs104893778
SNP Nexus

SNPshotrs104893778
SNPdbers104893778
MSV3drs104893778
GWAS Ctlgrs104893778
Max Magnitude0
OMIM180380
Desc
Variant0015
Relatedalso
ClinVar
Risk rs104893778(T;T)
Alt rs104893778(T;T)
Reference rs104893778(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129252544C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013904.17,