rs1055061
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1055061(A;A) |
Make rs1055061(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 23275723 |
Gene | HOMEZ |
is a | snp |
is | mentioned by |
dbSNP | rs1055061 |
dbSNP (classic) | rs1055061 |
ClinGen | rs1055061 |
ebi | rs1055061 |
HLI | rs1055061 |
Exac | rs1055061 |
Gnomad | rs1055061 |
Varsome | rs1055061 |
LitVar | rs1055061 |
Map | rs1055061 |
PheGenI | rs1055061 |
Biobank | rs1055061 |
1000 genomes | rs1055061 |
hgdp | rs1055061 |
ensembl | rs1055061 |
geneview | rs1055061 |
scholar | rs1055061 |
rs1055061 | |
pharmgkb | rs1055061 |
gwascentral | rs1055061 |
openSNP | rs1055061 |
23andMe | rs1055061 |
SNPshot | rs1055061 |
SNPdbe | rs1055061 |
MSV3d | rs1055061 |
GWAS Ctlg | rs1055061 |
GMAF | 0.0932 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20422016] Consanguinity mapping of congenital heart disease in a South Indian population