Have questions? Visit https://www.reddit.com/r/SNPedia

rs28933993

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28933993(A;C)
Make rs28933993(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position129532352
GeneRHO
is asnp
is mentioned by
dbSNPrs28933993
ebirs28933993
HLIrs28933993
Exacrs28933993
Varsomers28933993
Maprs28933993
PheGenIrs28933993
hapmaprs28933993
1000 genomesrs28933993
hgdprs28933993
ensemblrs28933993
gopubmedrs28933993
geneviewrs28933993
scholarrs28933993
googlers28933993
pharmgkbrs28933993
gwascentralrs28933993
openSNPrs28933993
23andMers28933993
23andMe allrs28933993
SNP Nexus

SNPshotrs28933993
SNPdbers28933993
MSV3drs28933993
GWAS Ctlgrs28933993
Max Magnitude0
OMIM180380
DescRETINITIS PIGMENTOSA 4
Variant0018
Relatedalso
Neighborrs28933995
Distance4
Neighborrs29001653
Distance370


ClinVar
Risk rs28933993(C;C)
Alt rs28933993(C;C)
Reference rs28933993(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129251195A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013901.24,