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rs121908143

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908143(G;G)
Make rs121908143(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position150972591
GeneCLRN1, CLRN1-AS1
is asnp
is mentioned by
dbSNPrs121908143
dbSNP (old)rs121908143
ClinGenrs121908143
ebirs121908143
HLIrs121908143
Exacrs121908143
Gnomadrs121908143
Varsomers121908143
Maprs121908143
PheGenIrs121908143
Biobankrs121908143
1000 genomesrs121908143
hgdprs121908143
ensemblrs121908143
gopubmedrs121908143
geneviewrs121908143
scholarrs121908143
googlers121908143
pharmgkbrs121908143
gwascentralrs121908143
openSNPrs121908143
23andMers121908143
23andMe allrs121908143
SNP Nexus

SNPshotrs121908143
SNPdbers121908143
MSV3drs121908143
GWAS Ctlgrs121908143
Max Magnitude0
OMIM606397
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121908143(G;G)
Alt rs121908143(G;G)
Reference Rs121908143(T;T)
Significance Pathogenic
Disease Usher syndrome not specified not provided
Variation info
Gene CLRN1-AS1 CLRN1
CLNDBN Usher syndrome, type 3A not specified not provided
Reversed 1
HGVS NC_000003.11:g.150690378A>C
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000004649.3, RCV000287738.1, RCV000414238.1,