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rs121913555

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913555(G;G)
Make rs121913555(G;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position51382430
GeneLIM2
is asnp
is mentioned by
dbSNPrs121913555
ebirs121913555
HLIrs121913555
Exacrs121913555
Varsomers121913555
Maprs121913555
PheGenIrs121913555
hapmaprs121913555
1000 genomesrs121913555
hgdprs121913555
ensemblrs121913555
gopubmedrs121913555
geneviewrs121913555
scholarrs121913555
googlers121913555
pharmgkbrs121913555
gwascentralrs121913555
openSNPrs121913555
23andMers121913555
23andMe allrs121913555
SNP Nexus

SNPshotrs121913555
SNPdbers121913555
MSV3drs121913555
GWAS Ctlgrs121913555
Max Magnitude0
OMIM154045
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121913555(G;G)
Alt rs121913555(G;G)
Reference rs121913555(T;T)
Significance Pathogenic
Disease Cataract 19
Variation info
Gene LIM2
CLNDBN Cataract 19, multiple types
Reversed 1
HGVS NC_000019.9:g.51885684A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015430.23,