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rs121908140

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908140(G;G)
Make rs121908140(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position150928107
GeneCLRN1
is asnp
is mentioned by
dbSNPrs121908140
ebirs121908140
HLIrs121908140
Exacrs121908140
Varsomers121908140
Maprs121908140
PheGenIrs121908140
hapmaprs121908140
1000 genomesrs121908140
hgdprs121908140
ensemblrs121908140
gopubmedrs121908140
geneviewrs121908140
scholarrs121908140
googlers121908140
pharmgkbrs121908140
gwascentralrs121908140
openSNPrs121908140
23andMers121908140
23andMe allrs121908140
SNP Nexus

SNPshotrs121908140
SNPdbers121908140
MSV3drs121908140
GWAS Ctlgrs121908140
GMAF0.0004591
Max Magnitude0
OMIM606397
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908140(C,G;C,G)
Alt rs121908140(C,G;C,G)
Reference rs121908140(T;T)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene CLRN1
CLNDBN Usher syndrome, type 3A
Reversed 1
HGVS NC_000003.11:g.150645894A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004642.4,