rs2095019
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2095019(A;A) |
Make rs2095019(A;C) |
Make rs2095019(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 169164779 |
Gene | LINC01615 |
is a | snp |
is | mentioned by |
dbSNP | rs2095019 |
dbSNP (classic) | rs2095019 |
ClinGen | rs2095019 |
ebi | rs2095019 |
HLI | rs2095019 |
Exac | rs2095019 |
Gnomad | rs2095019 |
Varsome | rs2095019 |
LitVar | rs2095019 |
Map | rs2095019 |
PheGenI | rs2095019 |
Biobank | rs2095019 |
1000 genomes | rs2095019 |
hgdp | rs2095019 |
ensembl | rs2095019 |
geneview | rs2095019 |
scholar | rs2095019 |
rs2095019 | |
pharmgkb | rs2095019 |
gwascentral | rs2095019 |
openSNP | rs2095019 |
23andMe | rs2095019 |
SNPshot | rs2095019 |
SNPdbe | rs2095019 |
MSV3d | rs2095019 |
GWAS Ctlg | rs2095019 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 24904231] A Novel Catechol-O-Methyltransferase Variant Associated with Human Disc Degeneration