rs144499152
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs144499152(C;C) |
Make rs144499152(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 206771211 |
Gene | FASTKD2 |
is a | snp |
is | mentioned by |
dbSNP | rs144499152 |
dbSNP (classic) | rs144499152 |
ClinGen | rs144499152 |
ebi | rs144499152 |
HLI | rs144499152 |
Exac | rs144499152 |
Gnomad | rs144499152 |
Varsome | rs144499152 |
LitVar | rs144499152 |
Map | rs144499152 |
PheGenI | rs144499152 |
Biobank | rs144499152 |
1000 genomes | rs144499152 |
hgdp | rs144499152 |
ensembl | rs144499152 |
geneview | rs144499152 |
scholar | rs144499152 |
rs144499152 | |
pharmgkb | rs144499152 |
gwascentral | rs144499152 |
openSNP | rs144499152 |
23andMe | rs144499152 |
SNPshot | rs144499152 |
SNPdbe | rs144499152 |
MSV3d | rs144499152 |
GWAS Ctlg | rs144499152 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs144499152(C;C) |
Alt | rs144499152(C;C) |
Reference | Rs144499152(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | FASTKD2 |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.207635935T>C |
CLNSRC | |
CLNACC | RCV000199763.2, RCV000401064.1, |