rs4744411
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4744411(A;A) |
Make rs4744411(A;G) |
Make rs4744411(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 94926763 |
Gene | C9orf3 |
is a | snp |
is | mentioned by |
dbSNP | rs4744411 |
dbSNP (classic) | rs4744411 |
ClinGen | rs4744411 |
ebi | rs4744411 |
HLI | rs4744411 |
Exac | rs4744411 |
Gnomad | rs4744411 |
Varsome | rs4744411 |
LitVar | rs4744411 |
Map | rs4744411 |
PheGenI | rs4744411 |
Biobank | rs4744411 |
1000 genomes | rs4744411 |
hgdp | rs4744411 |
ensembl | rs4744411 |
geneview | rs4744411 |
scholar | rs4744411 |
rs4744411 | |
pharmgkb | rs4744411 |
gwascentral | rs4744411 |
openSNP | rs4744411 |
23andMe | rs4744411 |
SNPshot | rs4744411 |
SNPdbe | rs4744411 |
MSV3d | rs4744411 |
GWAS Ctlg | rs4744411 |
GMAF | 0.3099 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19727120] Fine-Mapping of Vitiligo Susceptibility Loci on Chromosomes 7 and 9 and Interactions with NLRP1 (NALP1)