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rs137854863

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137854863(A;G)
Make rs137854863(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position74505102
GeneLTBP2
is asnp
is mentioned by
dbSNPrs137854863
dbSNP (classic)rs137854863
ClinGenrs137854863
ebirs137854863
HLIrs137854863
Exacrs137854863
Gnomadrs137854863
Varsomers137854863
LitVarrs137854863
Maprs137854863
PheGenIrs137854863
Biobankrs137854863
1000 genomesrs137854863
hgdprs137854863
ensemblrs137854863
geneviewrs137854863
scholarrs137854863
googlers137854863
pharmgkbrs137854863
gwascentralrs137854863
openSNPrs137854863
23andMers137854863
SNPshotrs137854863
SNPdbers137854863
MSV3drs137854863
GWAS Ctlgrs137854863
Max Magnitude0
ClinVar
Risk rs137854863(G;G)
Alt rs137854863(G;G)
Reference Rs137854863(A;A)
Significance Probable-Pathogenic
Disease Primary open angle glaucoma
Variation info
Gene LTBP2
CLNDBN Primary open angle glaucoma
Reversed 1
HGVS NC_000014.8:g.74971805T>C
CLNSRC ClinVar
CLNACC RCV000114812.1,