rs2027852
From SNPedia
Orientation | minus |
Stabilized | plus |
Make rs2027852(A;A) |
Make rs2027852(A;G) |
Make rs2027852(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 32576575 |
is a | snp |
is | mentioned by |
dbSNP | rs2027852 |
dbSNP (classic) | rs2027852 |
ClinGen | rs2027852 |
ebi | rs2027852 |
HLI | rs2027852 |
Exac | rs2027852 |
Gnomad | rs2027852 |
Varsome | rs2027852 |
LitVar | rs2027852 |
Map | rs2027852 |
PheGenI | rs2027852 |
Biobank | rs2027852 |
1000 genomes | rs2027852 |
hgdp | rs2027852 |
ensembl | rs2027852 |
geneview | rs2027852 |
scholar | rs2027852 |
rs2027852 | |
pharmgkb | rs2027852 |
gwascentral | rs2027852 |
openSNP | rs2027852 |
23andMe | rs2027852 |
SNPshot | rs2027852 |
SNPdbe | rs2027852 |
MSV3d | rs2027852 |
GWAS Ctlg | rs2027852 |
Max Magnitude | 0 |
[PMID 22536334] A genome-wide homozygosity association study identifies runs of homozygosity associated with rheumatoid arthritis in the human major histocompatibility complex