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rs29001637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs29001637(C;T)
Make rs29001637(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position129533710
GeneRHO
is asnp
is mentioned by
dbSNPrs29001637
ebirs29001637
HLIrs29001637
Exacrs29001637
Varsomers29001637
Maprs29001637
PheGenIrs29001637
hapmaprs29001637
1000 genomesrs29001637
hgdprs29001637
ensemblrs29001637
gopubmedrs29001637
geneviewrs29001637
scholarrs29001637
googlers29001637
pharmgkbrs29001637
gwascentralrs29001637
openSNPrs29001637
23andMers29001637
23andMe allrs29001637
SNP Nexus

SNPshotrs29001637
SNPdbers29001637
MSV3drs29001637
GWAS Ctlgrs29001637
Max Magnitude0
OMIM180380
DescRETINITIS PIGMENTOSA 4
Variant0003
Relatedalso
Neighborrs29001653
Distance988
Neighborrs29001566
Distance1


ClinVar
Risk rs29001637(T;T)
Alt rs29001637(T;T)
Reference rs29001637(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129252553C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013889.24,