rs1220869989
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 5 | Factor XI deficiency |
(T;C) | 3 | carrier of factor XI mutation |
(T;T) | 0 | common/normal |
Make rs1220869989(C;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 4 |
Position | 186276392 |
Gene | F11 |
is a | snp |
is | mentioned by |
dbSNP | rs1220869989 |
dbSNP (classic) | rs1220869989 |
ClinGen | rs1220869989 |
ebi | rs1220869989 |
HLI | rs1220869989 |
Exac | rs1220869989 |
Gnomad | rs1220869989 |
Varsome | rs1220869989 |
LitVar | rs1220869989 |
Map | rs1220869989 |
PheGenI | rs1220869989 |
Biobank | rs1220869989 |
1000 genomes | rs1220869989 |
hgdp | rs1220869989 |
ensembl | rs1220869989 |
geneview | rs1220869989 |
scholar | rs1220869989 |
rs1220869989 | |
pharmgkb | rs1220869989 |
gwascentral | rs1220869989 |
openSNP | rs1220869989 |
23andMe | rs1220869989 |
SNPshot | rs1220869989 |
SNPdbe | rs1220869989 |
MSV3d | rs1220869989 |
GWAS Ctlg | rs1220869989 |
Max Magnitude | 5 |
aka c.755+2T>C