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rs137854861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854861(C;T)
Make rs137854861(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position74552291
GeneLTBP2
is asnp
is mentioned by
dbSNPrs137854861
ebirs137854861
HLIrs137854861
Exacrs137854861
Varsomers137854861
Maprs137854861
PheGenIrs137854861
hapmaprs137854861
1000 genomesrs137854861
hgdprs137854861
ensemblrs137854861
gopubmedrs137854861
geneviewrs137854861
scholarrs137854861
googlers137854861
pharmgkbrs137854861
gwascentralrs137854861
openSNPrs137854861
23andMers137854861
23andMe allrs137854861
SNP Nexus

SNPshotrs137854861
SNPdbers137854861
MSV3drs137854861
GWAS Ctlgrs137854861
Max Magnitude0
ClinVar
Risk rs137854861(T;T)
Alt rs137854861(T;T)
Reference rs137854861(C;C)
Significance Probable-Pathogenic
Disease Pseudoexfoliation glaucoma
Variation info
Gene LTBP2
CLNDBN Pseudoexfoliation glaucoma
Reversed 1
HGVS NC_000014.8:g.75018994G>A
CLNSRC ClinVar
CLNACC RCV000114805.1,