rs2261722
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2261722(A;A) |
Make rs2261722(A;G) |
Make rs2261722(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 76254665 |
Gene | PCSK5 |
is a | snp |
is | mentioned by |
dbSNP | rs2261722 |
dbSNP (classic) | rs2261722 |
ClinGen | rs2261722 |
ebi | rs2261722 |
HLI | rs2261722 |
Exac | rs2261722 |
Gnomad | rs2261722 |
Varsome | rs2261722 |
LitVar | rs2261722 |
Map | rs2261722 |
PheGenI | rs2261722 |
Biobank | rs2261722 |
1000 genomes | rs2261722 |
hgdp | rs2261722 |
ensembl | rs2261722 |
geneview | rs2261722 |
scholar | rs2261722 |
rs2261722 | |
pharmgkb | rs2261722 |
gwascentral | rs2261722 |
openSNP | rs2261722 |
23andMe | rs2261722 |
SNPshot | rs2261722 |
SNPdbe | rs2261722 |
MSV3d | rs2261722 |
GWAS Ctlg | rs2261722 |
GMAF | 0.3127 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 23049896] Results of Genome-Wide Analyses on Neurodevelopmental Phenotypes at Four-Year Follow-Up following Cardiac Surgery in Infancy