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rs527236136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236136(-;-)
Make rs527236136(-;A)
ReferenceGRCh38 38.1/142
Chromosome1
Position216198429
GeneUSH2A
is asnp
is mentioned by
dbSNPrs527236136
ebirs527236136
HLIrs527236136
Exacrs527236136
Varsomers527236136
Maprs527236136
PheGenIrs527236136
hapmaprs527236136
1000 genomesrs527236136
hgdprs527236136
ensemblrs527236136
gopubmedrs527236136
geneviewrs527236136
scholarrs527236136
googlers527236136
pharmgkbrs527236136
gwascentralrs527236136
openSNPrs527236136
23andMers527236136
23andMe allrs527236136
SNP Nexus

SNPshotrs527236136
SNPdbers527236136
MSV3drs527236136
GWAS Ctlgrs527236136
Max Magnitude0
ClinVar
Risk rs527236136(;)
Alt rs527236136(;)
Reference rs527236136(A;A)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.216371771delT
CLNSRC ClinVar
CLNACC RCV000132712.1,