rs752097874
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs752097874(C;C) |
Make rs752097874(C;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 15 |
Position | 23645747 |
Gene | MAGEL2 |
is a | snp |
is | mentioned by |
dbSNP | rs752097874 |
dbSNP (classic) | rs752097874 |
ClinGen | rs752097874 |
ebi | rs752097874 |
HLI | rs752097874 |
Exac | rs752097874 |
Gnomad | rs752097874 |
Varsome | rs752097874 |
LitVar | rs752097874 |
Map | rs752097874 |
PheGenI | rs752097874 |
Biobank | rs752097874 |
1000 genomes | rs752097874 |
hgdp | rs752097874 |
ensembl | rs752097874 |
geneview | rs752097874 |
scholar | rs752097874 |
rs752097874 | |
pharmgkb | rs752097874 |
gwascentral | rs752097874 |
openSNP | rs752097874 |
23andMe | rs752097874 |
SNPshot | rs752097874 |
SNPdbe | rs752097874 |
MSV3d | rs752097874 |
GWAS Ctlg | rs752097874 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752097874(A;A) rs752097874(C;C) rs752097874(T;T) |
Alt | rs752097874(A;A) rs752097874(C;C) rs752097874(T;T) |
Reference | Rs752097874(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MAGEL2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.23890894G>A |
CLNSRC | |
CLNACC | RCV000254810.1, |