rs6700986
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6700986(A;A) |
Make rs6700986(A;G) |
Make rs6700986(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 180452403 |
Gene | ACBD6 |
is a | snp |
is | mentioned by |
dbSNP | rs6700986 |
dbSNP (classic) | rs6700986 |
ClinGen | rs6700986 |
ebi | rs6700986 |
HLI | rs6700986 |
Exac | rs6700986 |
Gnomad | rs6700986 |
Varsome | rs6700986 |
LitVar | rs6700986 |
Map | rs6700986 |
PheGenI | rs6700986 |
Biobank | rs6700986 |
1000 genomes | rs6700986 |
hgdp | rs6700986 |
ensembl | rs6700986 |
geneview | rs6700986 |
scholar | rs6700986 |
rs6700986 | |
pharmgkb | rs6700986 |
gwascentral | rs6700986 |
openSNP | rs6700986 |
23andMe | rs6700986 |
SNPshot | rs6700986 |
SNPdbe | rs6700986 |
MSV3d | rs6700986 |
GWAS Ctlg | rs6700986 |
GMAF | 0.4766 |
Max Magnitude | 0 |
[PMID 22215535] Association of nonalcoholic fatty liver disease with a single nucleotide polymorphism on the gene encoding leptin receptor