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rs527236101

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236101(A;A)
Make rs527236101(A;C)
ReferenceGRCh38 38.1/142
Chromosome3
Position129528913
GeneRHO
is asnp
is mentioned by
dbSNPrs527236101
ebirs527236101
HLIrs527236101
Exacrs527236101
Varsomers527236101
Maprs527236101
PheGenIrs527236101
hapmaprs527236101
1000 genomesrs527236101
hgdprs527236101
ensemblrs527236101
gopubmedrs527236101
geneviewrs527236101
scholarrs527236101
googlers527236101
pharmgkbrs527236101
gwascentralrs527236101
openSNPrs527236101
23andMers527236101
23andMe allrs527236101
SNP Nexus

SNPshotrs527236101
SNPdbers527236101
MSV3drs527236101
GWAS Ctlgrs527236101
Max Magnitude0
ClinVar
Risk rs527236101(A;A)
Alt rs527236101(A;A)
Reference rs527236101(C;C)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000003.11:g.129247756C>A
CLNSRC ClinVar
CLNACC RCV000132596.1,