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rs137854895

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854895(-;-)
Make rs137854895(-;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position74500974
GeneLTBP2
is asnp
is mentioned by
dbSNPrs137854895
ebirs137854895
HLIrs137854895
Exacrs137854895
Varsomers137854895
Maprs137854895
PheGenIrs137854895
hapmaprs137854895
1000 genomesrs137854895
hgdprs137854895
ensemblrs137854895
gopubmedrs137854895
geneviewrs137854895
scholarrs137854895
googlers137854895
pharmgkbrs137854895
gwascentralrs137854895
openSNPrs137854895
23andMers137854895
23andMe allrs137854895
SNP Nexus

SNPshotrs137854895
SNPdbers137854895
MSV3drs137854895
GWAS Ctlgrs137854895
Max Magnitude0
ClinVar
Risk rs137854895(;)
Alt rs137854895(;)
Reference rs137854895(C;C)
Significance Pathogenic
Disease Glaucoma
Variation info
Gene LTBP2
CLNDBN Glaucoma, congenital
Reversed 1
HGVS NC_000014.8:g.74967677delG
CLNSRC ClinVar
CLNACC RCV000114816.1,