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rs104893777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104893777(A;G)
Make rs104893777(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129532289
GeneRHO
is asnp
is mentioned by
dbSNPrs104893777
ebirs104893777
HLIrs104893777
Exacrs104893777
Varsomers104893777
Maprs104893777
PheGenIrs104893777
hapmaprs104893777
1000 genomesrs104893777
hgdprs104893777
ensemblrs104893777
gopubmedrs104893777
geneviewrs104893777
scholarrs104893777
googlers104893777
pharmgkbrs104893777
gwascentralrs104893777
openSNPrs104893777
23andMers104893777
23andMe allrs104893777
SNP Nexus

SNPshotrs104893777
SNPdbers104893777
MSV3drs104893777
GWAS Ctlgrs104893777
Max Magnitude0
OMIM180380
Desc
Variant0014
Relatedalso
ClinVar
Risk rs104893777(G;G)
Alt rs104893777(G;G)
Reference rs104893777(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129251132A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013900.23,