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rs869312732

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312732(A;A)
Make rs869312732(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position51380262
GeneLIM2
is asnp
is mentioned by
dbSNPrs869312732
ebirs869312732
HLIrs869312732
Exacrs869312732
Varsomers869312732
Maprs869312732
PheGenIrs869312732
hapmaprs869312732
1000 genomesrs869312732
hgdprs869312732
ensemblrs869312732
gopubmedrs869312732
geneviewrs869312732
scholarrs869312732
googlers869312732
pharmgkbrs869312732
gwascentralrs869312732
openSNPrs869312732
23andMers869312732
23andMe allrs869312732
SNP Nexus

SNPshotrs869312732
SNPdbers869312732
MSV3drs869312732
GWAS Ctlgrs869312732
Max Magnitude0
ClinVar
Risk rs869312732(A;A)
Alt rs869312732(A;A)
Reference rs869312732(G;G)
Significance Pathogenic
Disease Cataract 19
Variation info
Gene LIM2
CLNDBN Cataract 19, multiple types
Reversed 1
HGVS NC_000019.9:g.51883516C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000209996.1,