rs138556525
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs138556525(A;A) |
Make rs138556525(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 10 |
Position | 80275192 |
Gene | MAT1A |
is a | snp |
is | mentioned by |
dbSNP | rs138556525 |
dbSNP (classic) | rs138556525 |
ClinGen | rs138556525 |
ebi | rs138556525 |
HLI | rs138556525 |
Exac | rs138556525 |
Gnomad | rs138556525 |
Varsome | rs138556525 |
LitVar | rs138556525 |
Map | rs138556525 |
PheGenI | rs138556525 |
Biobank | rs138556525 |
1000 genomes | rs138556525 |
hgdp | rs138556525 |
ensembl | rs138556525 |
geneview | rs138556525 |
scholar | rs138556525 |
rs138556525 | |
pharmgkb | rs138556525 |
gwascentral | rs138556525 |
openSNP | rs138556525 |
23andMe | rs138556525 |
SNPshot | rs138556525 |
SNPdbe | rs138556525 |
MSV3d | rs138556525 |
GWAS Ctlg | rs138556525 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs138556525(A;A) rs138556525(C;C) |
Alt | rs138556525(A;A) rs138556525(C;C) |
Reference | Rs138556525(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MAT1A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.82034948G>A |
CLNSRC | |
CLNACC | RCV000376797.1, |