rs745368359
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs745368359(C;T) |
Make rs745368359(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 15544227 |
Gene | CYP4F22 |
is a | snp |
is | mentioned by |
dbSNP | rs745368359 |
dbSNP (classic) | rs745368359 |
ClinGen | rs745368359 |
ebi | rs745368359 |
HLI | rs745368359 |
Exac | rs745368359 |
Gnomad | rs745368359 |
Varsome | rs745368359 |
LitVar | rs745368359 |
Map | rs745368359 |
PheGenI | rs745368359 |
Biobank | rs745368359 |
1000 genomes | rs745368359 |
hgdp | rs745368359 |
ensembl | rs745368359 |
geneview | rs745368359 |
scholar | rs745368359 |
rs745368359 | |
pharmgkb | rs745368359 |
gwascentral | rs745368359 |
openSNP | rs745368359 |
23andMe | rs745368359 |
SNPshot | rs745368359 |
SNPdbe | rs745368359 |
MSV3d | rs745368359 |
GWAS Ctlg | rs745368359 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745368359(T;T) |
Alt | rs745368359(T;T) |
Reference | Rs745368359(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CYP4F22 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.15655038C>T |
CLNSRC | |
CLNACC | RCV000426277.1, |