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rs201493928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201493928(C;T)
Make rs201493928(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position54625068
GeneRP1
is asnp
is mentioned by
dbSNPrs201493928
ebirs201493928
HLIrs201493928
Exacrs201493928
Varsomers201493928
Maprs201493928
PheGenIrs201493928
hapmaprs201493928
1000 genomesrs201493928
hgdprs201493928
ensemblrs201493928
gopubmedrs201493928
geneviewrs201493928
scholarrs201493928
googlers201493928
pharmgkbrs201493928
gwascentralrs201493928
openSNPrs201493928
23andMers201493928
23andMe allrs201493928
SNP Nexus

SNPshotrs201493928
SNPdbers201493928
MSV3drs201493928
GWAS Ctlgrs201493928
Max Magnitude0
ClinVar
Risk rs201493928(T;T)
Alt rs201493928(T;T)
Reference rs201493928(C;C)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RP1
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000008.10:g.55537628C>T
CLNSRC ClinVar
CLNACC RCV000132658.1,