rs603769
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs603769(A;A) |
Make rs603769(A;G) |
Make rs603769(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 49492723 |
is a | snp |
is | mentioned by |
dbSNP | rs603769 |
dbSNP (classic) | rs603769 |
ClinGen | rs603769 |
ebi | rs603769 |
HLI | rs603769 |
Exac | rs603769 |
Gnomad | rs603769 |
Varsome | rs603769 |
LitVar | rs603769 |
Map | rs603769 |
PheGenI | rs603769 |
Biobank | rs603769 |
1000 genomes | rs603769 |
hgdp | rs603769 |
ensembl | rs603769 |
geneview | rs603769 |
scholar | rs603769 |
rs603769 | |
pharmgkb | rs603769 |
gwascentral | rs603769 |
openSNP | rs603769 |
23andMe | rs603769 |
SNPshot | rs603769 |
SNPdbe | rs603769 |
MSV3d | rs603769 |
GWAS Ctlg | rs603769 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25227100] Selection of human p75NTR tag SNPs and its biological significance for clinical association studies