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rs104893780

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893780(A;A)
Make rs104893780(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129532264
GeneRHO
is asnp
is mentioned by
dbSNPrs104893780
ebirs104893780
HLIrs104893780
Exacrs104893780
Varsomers104893780
Maprs104893780
PheGenIrs104893780
hapmaprs104893780
1000 genomesrs104893780
hgdprs104893780
ensemblrs104893780
gopubmedrs104893780
geneviewrs104893780
scholarrs104893780
googlers104893780
pharmgkbrs104893780
gwascentralrs104893780
openSNPrs104893780
23andMers104893780
23andMe allrs104893780
SNP Nexus

SNPshotrs104893780
SNPdbers104893780
MSV3drs104893780
GWAS Ctlgrs104893780
Max Magnitude0
OMIM180380
Desc
Variant0021
Relatedalso
ClinVar
Risk rs104893780(A;A)
Alt rs104893780(A;A)
Reference rs104893780(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129251107G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013908.17,