rs1057518614
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CT;CT) | 0 | common in clinvar |
Make rs1057518614(-;-) |
Make rs1057518614(-;CT) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 199272470 |
Gene | SATB2 |
is a | snp |
is | mentioned by |
dbSNP | rs1057518614 |
dbSNP (classic) | rs1057518614 |
ClinGen | rs1057518614 |
ebi | rs1057518614 |
HLI | rs1057518614 |
Exac | rs1057518614 |
Gnomad | rs1057518614 |
Varsome | rs1057518614 |
LitVar | rs1057518614 |
Map | rs1057518614 |
PheGenI | rs1057518614 |
Biobank | rs1057518614 |
1000 genomes | rs1057518614 |
hgdp | rs1057518614 |
ensembl | rs1057518614 |
geneview | rs1057518614 |
scholar | rs1057518614 |
rs1057518614 | |
pharmgkb | rs1057518614 |
gwascentral | rs1057518614 |
openSNP | rs1057518614 |
23andMe | rs1057518614 |
SNPshot | rs1057518614 |
SNPdbe | rs1057518614 |
MSV3d | rs1057518614 |
GWAS Ctlg | rs1057518614 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057518614(-;-) |
Alt | rs1057518614(-;-) |
Reference | Rs1057518614(CT;CT) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SATB2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000002.11:g.200137193_200137194delAG |
CLNSRC | |
CLNACC | RCV000413155.1, |