rs560588447
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common/normal |
(-;T) | 3 | Carrier of a prekallikrein deficiency mutation |
Make rs560588447(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 4 |
Position | 186236896 |
Gene | KLKB1 |
is a | snp |
is | mentioned by |
dbSNP | rs560588447 |
dbSNP (classic) | rs560588447 |
ClinGen | rs560588447 |
ebi | rs560588447 |
HLI | rs560588447 |
Exac | rs560588447 |
Gnomad | rs560588447 |
Varsome | rs560588447 |
LitVar | rs560588447 |
Map | rs560588447 |
PheGenI | rs560588447 |
Biobank | rs560588447 |
1000 genomes | rs560588447 |
hgdp | rs560588447 |
ensembl | rs560588447 |
geneview | rs560588447 |
scholar | rs560588447 |
rs560588447 | |
pharmgkb | rs560588447 |
gwascentral | rs560588447 |
openSNP | rs560588447 |
23andMe | rs560588447 |
SNPshot | rs560588447 |
SNPdbe | rs560588447 |
MSV3d | rs560588447 |
GWAS Ctlg | rs560588447 |
Max Magnitude | 3 |
Prekallikrein deficiency (recessive); aka c.451dupT
[PMID 26334176] This SNP is included in a curated list of mutations useful to include on an Ashkenazi Jews screening panel.