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rs121909145

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909145(C;G)
Make rs121909145(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position65546473
GeneLTBP3
is asnp
is mentioned by
dbSNPrs121909145
ebirs121909145
HLIrs121909145
Exacrs121909145
Varsomers121909145
Maprs121909145
PheGenIrs121909145
hapmaprs121909145
1000 genomesrs121909145
hgdprs121909145
ensemblrs121909145
gopubmedrs121909145
geneviewrs121909145
scholarrs121909145
googlers121909145
pharmgkbrs121909145
gwascentralrs121909145
openSNPrs121909145
23andMers121909145
23andMe allrs121909145
SNP Nexus

SNPshotrs121909145
SNPdbers121909145
MSV3drs121909145
GWAS Ctlgrs121909145
Max Magnitude0
OMIM602090
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909145(G,T;G,T)
Alt rs121909145(G,T;G,T)
Reference rs121909145(C;C)
Significance Pathogenic
Disease Verloes Bourguignon syndrome
Variation info
Gene LTBP3
CLNDBN Verloes Bourguignon syndrome
Reversed 1
HGVS NC_000011.9:g.65313944G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007997.3,