rs1057518092
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1057518092(A;A) |
Make rs1057518092(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 20 |
Position | 499909 |
Gene | CSNK2A1 |
is a | snp |
is | mentioned by |
dbSNP | rs1057518092 |
dbSNP (classic) | rs1057518092 |
ClinGen | rs1057518092 |
ebi | rs1057518092 |
HLI | rs1057518092 |
Exac | rs1057518092 |
Gnomad | rs1057518092 |
Varsome | rs1057518092 |
LitVar | rs1057518092 |
Map | rs1057518092 |
PheGenI | rs1057518092 |
Biobank | rs1057518092 |
1000 genomes | rs1057518092 |
hgdp | rs1057518092 |
ensembl | rs1057518092 |
geneview | rs1057518092 |
scholar | rs1057518092 |
rs1057518092 | |
pharmgkb | rs1057518092 |
gwascentral | rs1057518092 |
openSNP | rs1057518092 |
23andMe | rs1057518092 |
SNPshot | rs1057518092 |
SNPdbe | rs1057518092 |
MSV3d | rs1057518092 |
GWAS Ctlg | rs1057518092 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057518092(A;A) |
Alt | rs1057518092(A;A) |
Reference | Rs1057518092(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CSNK2A1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000020.10:g.480553C>T |
CLNSRC | |
CLNACC | RCV000413359.1, |