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

rs875989822

From SNPedia

Orientationminus
Geno Mag Summary
(TACCGGCTCAAAGC;TACCGGCTCAAAGC) 0 common in clinvar
Make rs875989822(-;-)
Make rs875989822(-;TACCGGCTCAAAGC)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position65547462
GeneLTBP3
is asnp
is mentioned by
dbSNPrs875989822
ebirs875989822
HLIrs875989822
Exacrs875989822
Varsomers875989822
Maprs875989822
PheGenIrs875989822
hapmaprs875989822
1000 genomesrs875989822
hgdprs875989822
ensemblrs875989822
gopubmedrs875989822
geneviewrs875989822
scholarrs875989822
googlers875989822
pharmgkbrs875989822
gwascentralrs875989822
openSNPrs875989822
23andMers875989822
23andMe allrs875989822
SNP Nexus

SNPshotrs875989822
SNPdbers875989822
MSV3drs875989822
GWAS Ctlgrs875989822
Max Magnitude0
ClinVar
Risk rs875989822(;)
Alt rs875989822(;)
Reference rs875989822(TACCGGCTCAAAGC;TACCGGCTCAAAGC)
Significance Pathogenic
Disease Verloes Bourguignon syndrome
Variation info
Gene LTBP3
CLNDBN Verloes Bourguignon syndrome
Reversed 1
HGVS NC_000011.9:g.65314933_65314946delGCTTTGAGCCGGTA
CLNSRC OMIM Allelic Variant
CLNACC RCV000186562.3,