rs72746635
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs72746635(A;A) |
Make rs72746635(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 60397390 |
Gene | ANXA2 |
is a | snp |
is | mentioned by |
dbSNP | rs72746635 |
dbSNP (classic) | rs72746635 |
ClinGen | rs72746635 |
ebi | rs72746635 |
HLI | rs72746635 |
Exac | rs72746635 |
Gnomad | rs72746635 |
Varsome | rs72746635 |
LitVar | rs72746635 |
Map | rs72746635 |
PheGenI | rs72746635 |
Biobank | rs72746635 |
1000 genomes | rs72746635 |
hgdp | rs72746635 |
ensembl | rs72746635 |
geneview | rs72746635 |
scholar | rs72746635 |
rs72746635 | |
pharmgkb | rs72746635 |
gwascentral | rs72746635 |
openSNP | rs72746635 |
23andMe | rs72746635 |
SNPshot | rs72746635 |
SNPdbe | rs72746635 |
MSV3d | rs72746635 |
GWAS Ctlg | rs72746635 |
GMAF | 0.02204 |
Max Magnitude | 0 |
[PMID 22822523] Effect of ANXA2 gene single nucleotide polymorphism (SNP) on the development of osteonecrosis in indian sickle cell patient: a PCR-RFLP approach