rs137853961
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs137853961(C;T) |
Make rs137853961(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 11113447 |
Gene | LDLR, MIR6886 |
is a | snp |
is | mentioned by |
dbSNP | rs137853961 |
dbSNP (classic) | rs137853961 |
ClinGen | rs137853961 |
ebi | rs137853961 |
HLI | rs137853961 |
Exac | rs137853961 |
Gnomad | rs137853961 |
Varsome | rs137853961 |
LitVar | rs137853961 |
Map | rs137853961 |
PheGenI | rs137853961 |
Biobank | rs137853961 |
1000 genomes | rs137853961 |
hgdp | rs137853961 |
ensembl | rs137853961 |
geneview | rs137853961 |
scholar | rs137853961 |
rs137853961 | |
pharmgkb | rs137853961 |
gwascentral | rs137853961 |
openSNP | rs137853961 |
23andMe | rs137853961 |
SNPshot | rs137853961 |
SNPdbe | rs137853961 |
MSV3d | rs137853961 |
GWAS Ctlg | rs137853961 |
Max Magnitude | 0 |
rs137853961, a SNP in the low density lipoprotein receptor LDLR gene that is also known as C452C, is being studied in participants in the NIH ClinSeq program. [PMID 19602640]
ClinVar | |
---|---|
Risk | rs137853961(T;T) |
Alt | rs137853961(T;T) |
Reference | Rs137853961(C;C) |
Significance | Untested |
Disease | not provided |
Variation | info |
Gene | LDLR MIR6886 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.11224123C>T |
CLNSRC | ClinVar |
CLNACC | RCV000058919.1, |