rs17849308
From SNPedia
Merged into | rs4680 |
Orientation | plus |
Stabilized | plus |
Make rs17849308(A;A) |
Make rs17849308(A;G) |
Make rs17849308(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 19963748 |
Gene | COMT, MIR4761 |
is a | snp |
is | mentioned by |
dbSNP | rs17849308 |
dbSNP (classic) | rs17849308 |
ClinGen | rs17849308 |
ebi | rs17849308 |
HLI | rs17849308 |
Exac | rs17849308 |
Gnomad | rs17849308 |
Varsome | rs17849308 |
LitVar | rs17849308 |
Map | rs17849308 |
PheGenI | rs17849308 |
Biobank | rs17849308 |
1000 genomes | rs17849308 |
hgdp | rs17849308 |
ensembl | rs17849308 |
geneview | rs17849308 |
scholar | rs17849308 |
rs17849308 | |
pharmgkb | rs17849308 |
gwascentral | rs17849308 |
openSNP | rs17849308 |
23andMe | rs17849308 |
SNPshot | rs17849308 |
SNPdbe | rs17849308 |
MSV3d | rs17849308 |
GWAS Ctlg | rs17849308 |
Status | Merged into rs4680 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
This is a mistaken rs#, apparently created by OMIM. It should refer to rs4680.