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rs111033434

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033434(A;A)
Make rs111033434(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position150972582
GeneCLRN1
is asnp
is mentioned by
dbSNPrs111033434
ebirs111033434
HLIrs111033434
Exacrs111033434
Varsomers111033434
Maprs111033434
PheGenIrs111033434
hapmaprs111033434
1000 genomesrs111033434
hgdprs111033434
ensemblrs111033434
gopubmedrs111033434
geneviewrs111033434
scholarrs111033434
googlers111033434
pharmgkbrs111033434
gwascentralrs111033434
openSNPrs111033434
23andMers111033434
23andMe allrs111033434
SNP Nexus

SNPshotrs111033434
SNPdbers111033434
MSV3drs111033434
GWAS Ctlgrs111033434
Max Magnitude0
ClinVar
Risk rs111033434(A;A)
Alt rs111033434(A;A)
Reference rs111033434(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene CLRN1-AS1 CLRN1
CLNDBN Usher syndrome, type 3A
Reversed 1
HGVS NC_000003.11:g.150690369C>T
CLNSRC ClinVar
CLNACC RCV000041430.2,