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rs527236117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236117(A;A)
Make rs527236117(A;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position35511648
GeneTULP1
is asnp
is mentioned by
dbSNPrs527236117
ebirs527236117
HLIrs527236117
Exacrs527236117
Varsomers527236117
Maprs527236117
PheGenIrs527236117
hapmaprs527236117
1000 genomesrs527236117
hgdprs527236117
ensemblrs527236117
gopubmedrs527236117
geneviewrs527236117
scholarrs527236117
googlers527236117
pharmgkbrs527236117
gwascentralrs527236117
openSNPrs527236117
23andMers527236117
23andMe allrs527236117
SNP Nexus

SNPshotrs527236117
SNPdbers527236117
MSV3drs527236117
GWAS Ctlgrs527236117
Max Magnitude0
ClinVar
Risk rs527236117(A;A)
Alt rs527236117(A;A)
Reference rs527236117(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene TULP1
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000006.11:g.35479425C>T
CLNSRC ClinVar
CLNACC RCV000132650.1,