rs6979
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6979(A;A) |
Make rs6979(A;G) |
Make rs6979(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 67657765 |
Gene | ACD, CARMIL2 |
is a | snp |
is | mentioned by |
dbSNP | rs6979 |
dbSNP (classic) | rs6979 |
ClinGen | rs6979 |
ebi | rs6979 |
HLI | rs6979 |
Exac | rs6979 |
Gnomad | rs6979 |
Varsome | rs6979 |
LitVar | rs6979 |
Map | rs6979 |
PheGenI | rs6979 |
Biobank | rs6979 |
1000 genomes | rs6979 |
hgdp | rs6979 |
ensembl | rs6979 |
geneview | rs6979 |
scholar | rs6979 |
rs6979 | |
pharmgkb | rs6979 |
gwascentral | rs6979 |
openSNP | rs6979 |
23andMe | rs6979 |
SNPshot | rs6979 |
SNPdbe | rs6979 |
MSV3d | rs6979 |
GWAS Ctlg | rs6979 |
GMAF | 0.4812 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19854717] The chromosome 16q region associated with ankylosing spondylitis includes the candidate gene tumour necrosis factor receptor type 1-associated death domain (TRADD)