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rs527236107

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236107(C;T)
Make rs527236107(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position10612126
GeneRP1L1
is asnp
is mentioned by
dbSNPrs527236107
ebirs527236107
HLIrs527236107
Exacrs527236107
Varsomers527236107
Maprs527236107
PheGenIrs527236107
hapmaprs527236107
1000 genomesrs527236107
hgdprs527236107
ensemblrs527236107
gopubmedrs527236107
geneviewrs527236107
scholarrs527236107
googlers527236107
pharmgkbrs527236107
gwascentralrs527236107
openSNPrs527236107
23andMers527236107
23andMe allrs527236107
SNP Nexus

SNPshotrs527236107
SNPdbers527236107
MSV3drs527236107
GWAS Ctlgrs527236107
Max Magnitude0
ClinVar
Risk rs527236107(T;T)
Alt rs527236107(T;T)
Reference rs527236107(C;C)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RP1L1
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000008.10:g.10469636G>A
CLNSRC ClinVar
CLNACC RCV000132695.1,