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

rs527236125

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236125(A;A)
Make rs527236125(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position215648660
GeneUSH2A
is asnp
is mentioned by
dbSNPrs527236125
ebirs527236125
HLIrs527236125
Exacrs527236125
Varsomers527236125
Maprs527236125
PheGenIrs527236125
hapmaprs527236125
1000 genomesrs527236125
hgdprs527236125
ensemblrs527236125
gopubmedrs527236125
geneviewrs527236125
scholarrs527236125
googlers527236125
pharmgkbrs527236125
gwascentralrs527236125
openSNPrs527236125
23andMers527236125
23andMe allrs527236125
SNP Nexus

SNPshotrs527236125
SNPdbers527236125
MSV3drs527236125
GWAS Ctlgrs527236125
Max Magnitude0
ClinVar
Risk rs527236125(A;A)
Alt rs527236125(A;A)
Reference rs527236125(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene USH2A
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000001.10:g.215822002C>T
CLNSRC ClinVar
CLNACC RCV000132707.1,