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rs875989823

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989823(G;T)
Make rs875989823(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position65551971
GeneLTBP3
is asnp
is mentioned by
dbSNPrs875989823
dbSNP (old)rs875989823
ClinGenrs875989823
ebirs875989823
HLIrs875989823
Exacrs875989823
Gnomadrs875989823
Varsomers875989823
Maprs875989823
PheGenIrs875989823
Biobankrs875989823
1000 genomesrs875989823
hgdprs875989823
ensemblrs875989823
gopubmedrs875989823
geneviewrs875989823
scholarrs875989823
googlers875989823
pharmgkbrs875989823
gwascentralrs875989823
openSNPrs875989823
23andMers875989823
23andMe allrs875989823
SNP Nexus

SNPshotrs875989823
SNPdbers875989823
MSV3drs875989823
GWAS Ctlgrs875989823
Max Magnitude0
ClinVar
Risk rs875989823(T;T)
Alt rs875989823(T;T)
Reference Rs875989823(G;G)
Significance Pathogenic
Disease Verloes Bourguignon syndrome
Variation info
Gene LTBP3
CLNDBN Verloes Bourguignon syndrome
Reversed 1
HGVS NC_000011.9:g.65319442C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000186564.2,