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rs869320618

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320618(A;A)
Make rs869320618(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position129530996
GeneRHO
is asnp
is mentioned by
dbSNPrs869320618
ebirs869320618
HLIrs869320618
Exacrs869320618
Varsomers869320618
Maprs869320618
PheGenIrs869320618
hapmaprs869320618
1000 genomesrs869320618
hgdprs869320618
ensemblrs869320618
gopubmedrs869320618
geneviewrs869320618
scholarrs869320618
googlers869320618
pharmgkbrs869320618
gwascentralrs869320618
openSNPrs869320618
23andMers869320618
23andMe allrs869320618
SNP Nexus

SNPshotrs869320618
SNPdbers869320618
MSV3drs869320618
GWAS Ctlgrs869320618
Max Magnitude0
ClinVar
Risk rs869320618(A;A)
Alt rs869320618(A;A)
Reference rs869320618(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4, autosomal recessive
Reversed 0
HGVS NC_000003.11:g.129249839G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022756.25,