Have questions? Visit https://www.reddit.com/r/SNPedia

rs527236124

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236124(G;T)
Make rs527236124(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position215671258
GeneUSH2A
is asnp
is mentioned by
dbSNPrs527236124
ebirs527236124
HLIrs527236124
Exacrs527236124
Varsomers527236124
Maprs527236124
PheGenIrs527236124
hapmaprs527236124
1000 genomesrs527236124
hgdprs527236124
ensemblrs527236124
gopubmedrs527236124
geneviewrs527236124
scholarrs527236124
googlers527236124
pharmgkbrs527236124
gwascentralrs527236124
openSNPrs527236124
23andMers527236124
23andMe allrs527236124
SNP Nexus

SNPshotrs527236124
SNPdbers527236124
MSV3drs527236124
GWAS Ctlgrs527236124
Max Magnitude0
ClinVar
Risk rs527236124(T;T)
Alt rs527236124(T;T)
Reference rs527236124(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene USH2A
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000001.10:g.215844600C>A
CLNSRC ClinVar
CLNACC RCV000132705.1,