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rs104893786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104893786(A;G)
Make rs104893786(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129528777
GeneRHO
is asnp
is mentioned by
dbSNPrs104893786
ebirs104893786
HLIrs104893786
Exacrs104893786
Varsomers104893786
Maprs104893786
PheGenIrs104893786
hapmaprs104893786
1000 genomesrs104893786
hgdprs104893786
ensemblrs104893786
gopubmedrs104893786
geneviewrs104893786
scholarrs104893786
googlers104893786
pharmgkbrs104893786
gwascentralrs104893786
openSNPrs104893786
23andMers104893786
23andMe allrs104893786
SNP Nexus

SNPshotrs104893786
SNPdbers104893786
MSV3drs104893786
GWAS Ctlgrs104893786
Max Magnitude0
OMIM180380
Desc
Variant0029
Relatedalso
ClinVar
Risk rs104893786(G;G)
Alt rs104893786(G;G)
Reference rs104893786(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 4 Retinitis pigmentosa
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4 Retinitis pigmentosa
Reversed 0
HGVS NC_000003.11:g.129247620A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013917.24, RCV000132598.1,