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rs527236118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236118(C;C)
Make rs527236118(C;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position215799114
GeneUSH2A
is asnp
is mentioned by
dbSNPrs527236118
ebirs527236118
HLIrs527236118
Exacrs527236118
Varsomers527236118
Maprs527236118
PheGenIrs527236118
hapmaprs527236118
1000 genomesrs527236118
hgdprs527236118
ensemblrs527236118
gopubmedrs527236118
geneviewrs527236118
scholarrs527236118
googlers527236118
pharmgkbrs527236118
gwascentralrs527236118
openSNPrs527236118
23andMers527236118
23andMe allrs527236118
SNP Nexus

SNPshotrs527236118
SNPdbers527236118
MSV3drs527236118
GWAS Ctlgrs527236118
Max Magnitude0
ClinVar
Risk rs527236118(C;C)
Alt rs527236118(C;C)
Reference rs527236118(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene USH2A
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000001.10:g.215972456A>G
CLNSRC ClinVar
CLNACC RCV000132717.1,