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rs137854860

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854860(A;A)
Make rs137854860(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position74502911
GeneLTBP2
is asnp
is mentioned by
dbSNPrs137854860
ebirs137854860
HLIrs137854860
Exacrs137854860
Varsomers137854860
Maprs137854860
PheGenIrs137854860
hapmaprs137854860
1000 genomesrs137854860
hgdprs137854860
ensemblrs137854860
gopubmedrs137854860
geneviewrs137854860
scholarrs137854860
googlers137854860
pharmgkbrs137854860
gwascentralrs137854860
openSNPrs137854860
23andMers137854860
23andMe allrs137854860
SNP Nexus

SNPshotrs137854860
SNPdbers137854860
MSV3drs137854860
GWAS Ctlgrs137854860
Max Magnitude0
ClinVar
Risk rs137854860(A;A)
Alt rs137854860(A;A)
Reference rs137854860(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.74969614C>T
CLNSRC ClinVar
CLNACC RCV000114815.1,