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

rs878853036

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853036(C;T)
Make rs878853036(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position65540034
GeneLTBP3
is asnp
is mentioned by
dbSNPrs878853036
dbSNP (classic)rs878853036
ClinGenrs878853036
ebirs878853036
HLIrs878853036
Exacrs878853036
Gnomadrs878853036
Varsomers878853036
LitVarrs878853036
Maprs878853036
PheGenIrs878853036
Biobankrs878853036
1000 genomesrs878853036
hgdprs878853036
ensemblrs878853036
geneviewrs878853036
scholarrs878853036
googlers878853036
pharmgkbrs878853036
gwascentralrs878853036
openSNPrs878853036
23andMers878853036
SNPshotrs878853036
SNPdbers878853036
MSV3drs878853036
GWAS Ctlgrs878853036
Max Magnitude0
ClinVar
Risk rs878853036(T;T)
Alt rs878853036(T;T)
Reference Rs878853036(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LTBP3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.65307505G>A
CLNSRC
CLNACC RCV000224415.1,