rs6960920
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6960920(C;C) |
Make rs6960920(C;G) |
Make rs6960920(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 44376473 |
is a | snp |
is | mentioned by |
dbSNP | rs6960920 |
dbSNP (classic) | rs6960920 |
ClinGen | rs6960920 |
ebi | rs6960920 |
HLI | rs6960920 |
Exac | rs6960920 |
Gnomad | rs6960920 |
Varsome | rs6960920 |
LitVar | rs6960920 |
Map | rs6960920 |
PheGenI | rs6960920 |
Biobank | rs6960920 |
1000 genomes | rs6960920 |
hgdp | rs6960920 |
ensembl | rs6960920 |
geneview | rs6960920 |
scholar | rs6960920 |
rs6960920 | |
pharmgkb | rs6960920 |
gwascentral | rs6960920 |
openSNP | rs6960920 |
23andMe | rs6960920 |
SNPshot | rs6960920 |
SNPdbe | rs6960920 |
MSV3d | rs6960920 |
GWAS Ctlg | rs6960920 |
GMAF | 0.4252 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
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[PMID 19727120] Fine-Mapping of Vitiligo Susceptibility Loci on Chromosomes 7 and 9 and Interactions with NLRP1 (NALP1)