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rs28933395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28933395(C;G)
Make rs28933395(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129528891
GeneRHO
is asnp
is mentioned by
dbSNPrs28933395
ebirs28933395
HLIrs28933395
Exacrs28933395
Varsomers28933395
Maprs28933395
PheGenIrs28933395
hapmaprs28933395
1000 genomesrs28933395
hgdprs28933395
ensemblrs28933395
gopubmedrs28933395
geneviewrs28933395
scholarrs28933395
googlers28933395
pharmgkbrs28933395
gwascentralrs28933395
openSNPrs28933395
23andMers28933395
23andMe allrs28933395
SNP Nexus

SNPshotrs28933395
SNPdbers28933395
MSV3drs28933395
GWAS Ctlgrs28933395
Max Magnitude0
OMIM180380
DescRETINITIS PIGMENTOSA 4
Variant0024
Relatedalso
Neighborrs28933394
Distance15


ClinVar
Risk rs28933395(G;G)
Alt rs28933395(G;G)
Reference rs28933395(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129247734C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013912.24,