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rs527236122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236122(C;G)
Make rs527236122(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position215634523
GeneUSH2A
is asnp
is mentioned by
dbSNPrs527236122
ebirs527236122
HLIrs527236122
Exacrs527236122
Varsomers527236122
Maprs527236122
PheGenIrs527236122
hapmaprs527236122
1000 genomesrs527236122
hgdprs527236122
ensemblrs527236122
gopubmedrs527236122
geneviewrs527236122
scholarrs527236122
googlers527236122
pharmgkbrs527236122
gwascentralrs527236122
openSNPrs527236122
23andMers527236122
23andMe allrs527236122
SNP Nexus

SNPshotrs527236122
SNPdbers527236122
MSV3drs527236122
GWAS Ctlgrs527236122
Max Magnitude0
ClinVar
Risk rs527236122(G;G)
Alt rs527236122(G;G)
Reference rs527236122(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene USH2A
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000001.10:g.215807865G>C
CLNSRC ClinVar
CLNACC RCV000132708.1,