rs17419032
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17419032(C;C) |
Make rs17419032(C;T) |
Make rs17419032(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 201029403 |
Gene | LOC101929305 |
is a | snp |
is | mentioned by |
dbSNP | rs17419032 |
dbSNP (classic) | rs17419032 |
ClinGen | rs17419032 |
ebi | rs17419032 |
HLI | rs17419032 |
Exac | rs17419032 |
Gnomad | rs17419032 |
Varsome | rs17419032 |
LitVar | rs17419032 |
Map | rs17419032 |
PheGenI | rs17419032 |
Biobank | rs17419032 |
1000 genomes | rs17419032 |
hgdp | rs17419032 |
ensembl | rs17419032 |
geneview | rs17419032 |
scholar | rs17419032 |
rs17419032 | |
pharmgkb | rs17419032 |
gwascentral | rs17419032 |
openSNP | rs17419032 |
23andMe | rs17419032 |
SNPshot | rs17419032 |
SNPdbe | rs17419032 |
MSV3d | rs17419032 |
GWAS Ctlg | rs17419032 |
GMAF | 0.1396 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20007504] Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci.