rs1373494
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1373494(A;A) |
Make rs1373494(A;C) |
Make rs1373494(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 33746904 |
is a | snp |
is | mentioned by |
dbSNP | rs1373494 |
dbSNP (classic) | rs1373494 |
ClinGen | rs1373494 |
ebi | rs1373494 |
HLI | rs1373494 |
Exac | rs1373494 |
Gnomad | rs1373494 |
Varsome | rs1373494 |
LitVar | rs1373494 |
Map | rs1373494 |
PheGenI | rs1373494 |
Biobank | rs1373494 |
1000 genomes | rs1373494 |
hgdp | rs1373494 |
ensembl | rs1373494 |
geneview | rs1373494 |
scholar | rs1373494 |
rs1373494 | |
pharmgkb | rs1373494 |
gwascentral | rs1373494 |
openSNP | rs1373494 |
23andMe | rs1373494 |
SNPshot | rs1373494 |
SNPdbe | rs1373494 |
MSV3d | rs1373494 |
GWAS Ctlg | rs1373494 |
GMAF | 0.264 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 18205893] Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations.