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rs137854855

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854855(C;T)
Make rs137854855(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position74551108
GeneLTBP2
is asnp
is mentioned by
dbSNPrs137854855
ebirs137854855
HLIrs137854855
Exacrs137854855
Varsomers137854855
Maprs137854855
PheGenIrs137854855
hapmaprs137854855
1000 genomesrs137854855
hgdprs137854855
ensemblrs137854855
gopubmedrs137854855
geneviewrs137854855
scholarrs137854855
googlers137854855
pharmgkbrs137854855
gwascentralrs137854855
openSNPrs137854855
23andMers137854855
23andMe allrs137854855
SNP Nexus

SNPshotrs137854855
SNPdbers137854855
MSV3drs137854855
GWAS Ctlgrs137854855
Max Magnitude0
ClinVar
Risk rs137854855(T;T)
Alt rs137854855(T;T)
Reference rs137854855(C;C)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene LTBP2
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000014.8:g.75017811G>A
CLNSRC ClinVar
CLNACC RCV000114808.1,