Have questions? Visit https://www.reddit.com/r/SNPedia

rs104893771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893771(A;A)
Make rs104893771(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position129528993
GeneRHO
is asnp
is mentioned by
dbSNPrs104893771
ebirs104893771
HLIrs104893771
Exacrs104893771
Varsomers104893771
Maprs104893771
PheGenIrs104893771
hapmaprs104893771
1000 genomesrs104893771
hgdprs104893771
ensemblrs104893771
gopubmedrs104893771
geneviewrs104893771
scholarrs104893771
googlers104893771
pharmgkbrs104893771
gwascentralrs104893771
openSNPrs104893771
23andMers104893771
23andMe allrs104893771
SNP Nexus

SNPshotrs104893771
SNPdbers104893771
MSV3drs104893771
GWAS Ctlgrs104893771
Max Magnitude0
OMIM180380
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104893771(A;A)
Alt rs104893771(A;A)
Reference rs104893771(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129247836T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013894.24,