rs141212743
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs141212743(C;T) |
Make rs141212743(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 12181337 |
Gene | LRP6 |
is a | snp |
is | mentioned by |
dbSNP | rs141212743 |
dbSNP (classic) | rs141212743 |
ClinGen | rs141212743 |
ebi | rs141212743 |
HLI | rs141212743 |
Exac | rs141212743 |
Gnomad | rs141212743 |
Varsome | rs141212743 |
LitVar | rs141212743 |
Map | rs141212743 |
PheGenI | rs141212743 |
Biobank | rs141212743 |
1000 genomes | rs141212743 |
hgdp | rs141212743 |
ensembl | rs141212743 |
geneview | rs141212743 |
scholar | rs141212743 |
rs141212743 | |
pharmgkb | rs141212743 |
gwascentral | rs141212743 |
openSNP | rs141212743 |
23andMe | rs141212743 |
SNPshot | rs141212743 |
SNPdbe | rs141212743 |
MSV3d | rs141212743 |
GWAS Ctlg | rs141212743 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141212743(T;T) |
Alt | rs141212743(T;T) |
Reference | Rs141212743(C;C) |
Significance | Pathogenic |
Disease | Coronary artery disease |
Variation | info |
Gene | LRP6 |
CLNDBN | Coronary artery disease, autosomal dominant 2 |
Reversed | 0 |
HGVS | NC_000012.11:g.12334271C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000056294.2, |