rs913435613
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs913435613(C;C) |
Make rs913435613(C;T) |
Make rs913435613(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 80276381 |
Gene | MAT1A |
is a | snp |
is | mentioned by |
dbSNP | rs913435613 |
dbSNP (classic) | rs913435613 |
ClinGen | rs913435613 |
ebi | rs913435613 |
HLI | rs913435613 |
Exac | rs913435613 |
Gnomad | rs913435613 |
Varsome | rs913435613 |
LitVar | rs913435613 |
Map | rs913435613 |
PheGenI | rs913435613 |
Biobank | rs913435613 |
1000 genomes | rs913435613 |
hgdp | rs913435613 |
ensembl | rs913435613 |
geneview | rs913435613 |
scholar | rs913435613 |
rs913435613 | |
pharmgkb | rs913435613 |
gwascentral | rs913435613 |
openSNP | rs913435613 |
23andMe | rs913435613 |
SNPshot | rs913435613 |
SNPdbe | rs913435613 |
MSV3d | rs913435613 |
GWAS Ctlg | rs913435613 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs913435613(A;A) |
Alt | rs913435613(A;A) |
Reference | Rs913435613(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MAT1A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.82036137G>A |
CLNSRC | |
CLNACC | RCV000433867.1, |