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rs104893772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893772(A;A)
Make rs104893772(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129528999
GeneRHO
is asnp
is mentioned by
dbSNPrs104893772
ebirs104893772
HLIrs104893772
Exacrs104893772
Varsomers104893772
Maprs104893772
PheGenIrs104893772
hapmaprs104893772
1000 genomesrs104893772
hgdprs104893772
ensemblrs104893772
gopubmedrs104893772
geneviewrs104893772
scholarrs104893772
googlers104893772
pharmgkbrs104893772
gwascentralrs104893772
openSNPrs104893772
23andMers104893772
23andMe allrs104893772
SNP Nexus

SNPshotrs104893772
SNPdbers104893772
MSV3drs104893772
GWAS Ctlgrs104893772
Max Magnitude0
OMIM180380
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104893772(A;A)
Alt rs104893772(A;A)
Reference rs104893772(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129247842G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013895.17,