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rs875989824

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989824(-;-)
Make rs875989824(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position65543547
GeneLTBP3
is asnp
is mentioned by
dbSNPrs875989824
ebirs875989824
HLIrs875989824
Exacrs875989824
Varsomers875989824
Maprs875989824
PheGenIrs875989824
hapmaprs875989824
1000 genomesrs875989824
hgdprs875989824
ensemblrs875989824
gopubmedrs875989824
geneviewrs875989824
scholarrs875989824
googlers875989824
pharmgkbrs875989824
gwascentralrs875989824
openSNPrs875989824
23andMers875989824
23andMe allrs875989824
SNP Nexus

SNPshotrs875989824
SNPdbers875989824
MSV3drs875989824
GWAS Ctlgrs875989824
Max Magnitude0
ClinVar
Risk rs875989824(;)
Alt rs875989824(;)
Reference rs875989824(G;G)
Significance Pathogenic
Disease Verloes Bourguignon syndrome
Variation info
Gene LTBP3
CLNDBN Verloes Bourguignon syndrome
Reversed 1
HGVS NC_000011.9:g.65311018delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000186566.2,