Have questions? Visit https://www.reddit.com/r/SNPedia

rs137854856

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854856(A;A)
Make rs137854856(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position74508727
GeneLTBP2
is asnp
is mentioned by
dbSNPrs137854856
ebirs137854856
HLIrs137854856
Exacrs137854856
Varsomers137854856
Maprs137854856
PheGenIrs137854856
hapmaprs137854856
1000 genomesrs137854856
hgdprs137854856
ensemblrs137854856
gopubmedrs137854856
geneviewrs137854856
scholarrs137854856
googlers137854856
pharmgkbrs137854856
gwascentralrs137854856
openSNPrs137854856
23andMers137854856
23andMe allrs137854856
SNP Nexus

SNPshotrs137854856
SNPdbers137854856
MSV3drs137854856
GWAS Ctlgrs137854856
Max Magnitude0
ClinVar
Risk rs137854856(A;A)
Alt rs137854856(A;A)
Reference rs137854856(G;G)
Significance Pathogenic
Disease Weill-Marchesani syndrome 3 Weill-Marchesani syndrome 1
Variation info
Gene LTBP2
CLNDBN Weill-Marchesani syndrome 3 Weill-Marchesani syndrome 1
Reversed 1
HGVS NC_000014.8:g.74975430C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030740.2, RCV000114810.1,