rs1057521726
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1057521726(G;T) |
Make rs1057521726(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 4 |
Position | 79983913 |
Gene | ANTXR2 |
is a | snp |
is | mentioned by |
dbSNP | rs1057521726 |
dbSNP (old) | rs1057521726 |
ClinGen | rs1057521726 |
ebi | rs1057521726 |
HLI | rs1057521726 |
Exac | rs1057521726 |
Gnomad | rs1057521726 |
Varsome | rs1057521726 |
Map | rs1057521726 |
PheGenI | rs1057521726 |
Biobank | rs1057521726 |
1000 genomes | rs1057521726 |
hgdp | rs1057521726 |
ensembl | rs1057521726 |
gopubmed | rs1057521726 |
geneview | rs1057521726 |
scholar | rs1057521726 |
rs1057521726 | |
pharmgkb | rs1057521726 |
gwascentral | rs1057521726 |
openSNP | rs1057521726 |
23andMe | rs1057521726 |
23andMe all | rs1057521726 |
SNPshot | rs1057521726 |
SNPdbe | rs1057521726 |
MSV3d | rs1057521726 |
GWAS Ctlg | rs1057521726 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057521726(T;T) |
Alt | rs1057521726(T;T) |
Reference | Rs1057521726(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ANTXR2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000004.11:g.80905067C>A |
CLNSRC | |
CLNACC | RCV000433418.1, |