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rs137854862

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854862(A;A)
Make rs137854862(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position74508685
GeneLTBP2
is asnp
is mentioned by
dbSNPrs137854862
ebirs137854862
HLIrs137854862
Exacrs137854862
Varsomers137854862
Maprs137854862
PheGenIrs137854862
hapmaprs137854862
1000 genomesrs137854862
hgdprs137854862
ensemblrs137854862
gopubmedrs137854862
geneviewrs137854862
scholarrs137854862
googlers137854862
pharmgkbrs137854862
gwascentralrs137854862
openSNPrs137854862
23andMers137854862
23andMe allrs137854862
SNP Nexus

SNPshotrs137854862
SNPdbers137854862
MSV3drs137854862
GWAS Ctlgrs137854862
Max Magnitude0
ClinVar
Risk rs137854862(A;A)
Alt rs137854862(A;A)
Reference rs137854862(G;G)
Significance Probable-Pathogenic
Disease Primary open angle glaucoma
Variation info
Gene LTBP2
CLNDBN Primary open angle glaucoma
Reversed 1
HGVS NC_000014.8:g.74975388C>T
CLNSRC ClinVar
CLNACC RCV000114811.1,