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rs29001653

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs29001653(A;G)
Make rs29001653(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129532722
GeneRHO
is asnp
is mentioned by
dbSNPrs29001653
ebirs29001653
HLIrs29001653
Exacrs29001653
Varsomers29001653
Maprs29001653
PheGenIrs29001653
hapmaprs29001653
1000 genomesrs29001653
hgdprs29001653
ensemblrs29001653
gopubmedrs29001653
geneviewrs29001653
scholarrs29001653
googlers29001653
pharmgkbrs29001653
gwascentralrs29001653
openSNPrs29001653
23andMers29001653
23andMe allrs29001653
SNP Nexus

SNPshotrs29001653
SNPdbers29001653
MSV3drs29001653
GWAS Ctlgrs29001653
Max Magnitude0
OMIM180380
DescRETINITIS PIGMENTOSA 4
Variant0016
Relatedalso
Neighborrs28933993
Distance370
Neighborrs29001637
Distance988


ClinVar
Risk rs29001653(G;G)
Alt rs29001653(G;G)
Reference rs29001653(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129251565A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013905.23,