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rs28933394

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28933394(C;G)
Make rs28933394(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129528906
GeneRHO
is asnp
is mentioned by
dbSNPrs28933394
ebirs28933394
HLIrs28933394
Exacrs28933394
Varsomers28933394
Maprs28933394
PheGenIrs28933394
hapmaprs28933394
1000 genomesrs28933394
hgdprs28933394
ensemblrs28933394
gopubmedrs28933394
geneviewrs28933394
scholarrs28933394
googlers28933394
pharmgkbrs28933394
gwascentralrs28933394
openSNPrs28933394
23andMers28933394
23andMe allrs28933394
SNP Nexus

SNPshotrs28933394
SNPdbers28933394
MSV3drs28933394
GWAS Ctlgrs28933394
Max Magnitude0
OMIM180380
DescRETINITIS PIGMENTOSA 4
Variant0004
Relatedalso
Neighborrs28933395
Distance15
Neighborrs28933994
Distance151


ClinVar
Risk rs28933394(G,T;G,T)
Alt rs28933394(G,T;G,T)
Reference rs28933394(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129247749C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013890.23,