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rs878853262

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853262(-;-)
Make rs878853262(-;G)
Make rs878853262(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position65547808
GeneLTBP3
is asnp
is mentioned by
dbSNPrs878853262
ebirs878853262
HLIrs878853262
Exacrs878853262
Varsomers878853262
Maprs878853262
PheGenIrs878853262
hapmaprs878853262
1000 genomesrs878853262
hgdprs878853262
ensemblrs878853262
gopubmedrs878853262
geneviewrs878853262
scholarrs878853262
googlers878853262
pharmgkbrs878853262
gwascentralrs878853262
openSNPrs878853262
23andMers878853262
23andMe allrs878853262
SNP Nexus

SNPshotrs878853262
SNPdbers878853262
MSV3drs878853262
GWAS Ctlgrs878853262
Max Magnitude0
ClinVar
Risk rs878853262(G;G)
Alt rs878853262(G;G)
Reference rs878853262(;)
Significance Pathogenic
Disease Verloes Bourguignon syndrome
Variation info
Gene LTBP3
CLNDBN Verloes Bourguignon syndrome
Reversed 1
HGVS NC_000011.9:g.65315280dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000186561.3,