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rs104893776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104893776(A;G)
Make rs104893776(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position129532253
GeneRHO
is asnp
is mentioned by
dbSNPrs104893776
ebirs104893776
HLIrs104893776
Exacrs104893776
Varsomers104893776
Maprs104893776
PheGenIrs104893776
hapmaprs104893776
1000 genomesrs104893776
hgdprs104893776
ensemblrs104893776
gopubmedrs104893776
geneviewrs104893776
scholarrs104893776
googlers104893776
pharmgkbrs104893776
gwascentralrs104893776
openSNPrs104893776
23andMers104893776
23andMe allrs104893776
SNP Nexus

SNPshotrs104893776
SNPdbers104893776
MSV3drs104893776
GWAS Ctlgrs104893776
Max Magnitude0
OMIM180380
Desc
Variant0013
Relatedalso
ClinVar
Risk rs104893776(G;G)
Alt rs104893776(G;G)
Reference rs104893776(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 4
Variation info
Gene RHO
CLNDBN Retinitis pigmentosa 4
Reversed 0
HGVS NC_000003.11:g.129251096A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013899.24,