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rs104893768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893768(A;A)
Make rs104893768(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position129528801
GeneRHO
is asnp
is mentioned by
dbSNPrs104893768
ebirs104893768
HLIrs104893768
Exacrs104893768
Varsomers104893768
Maprs104893768
PheGenIrs104893768
hapmaprs104893768
1000 genomesrs104893768
hgdprs104893768
ensemblrs104893768
gopubmedrs104893768
geneviewrs104893768
scholarrs104893768
googlers104893768
pharmgkbrs104893768
gwascentralrs104893768
openSNPrs104893768
23andMers104893768
23andMe allrs104893768
SNP Nexus

SNPshotrs104893768
SNPdbers104893768
MSV3drs104893768
GWAS Ctlgrs104893768
Max Magnitude0
OMIM180380
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893768(A;A)
Alt rs104893768(A;A)
Reference rs104893768(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129247644C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013887.17,