rs727504022
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 8.8 | Methylmalonic aciduria (predicted) |
(A;G) | 3 | Carrier for a methylmalonic aciduria mutation |
(G;G) | 0 | common in clinvar |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 49459187 |
Gene | MUT |
is a | snp |
is | mentioned by |
dbSNP | rs727504022 |
dbSNP (classic) | rs727504022 |
ClinGen | rs727504022 |
ebi | rs727504022 |
HLI | rs727504022 |
Exac | rs727504022 |
Gnomad | rs727504022 |
Varsome | rs727504022 |
LitVar | rs727504022 |
Map | rs727504022 |
PheGenI | rs727504022 |
Biobank | rs727504022 |
1000 genomes | rs727504022 |
hgdp | rs727504022 |
ensembl | rs727504022 |
geneview | rs727504022 |
scholar | rs727504022 |
rs727504022 | |
pharmgkb | rs727504022 |
gwascentral | rs727504022 |
openSNP | rs727504022 |
23andMe | rs727504022 |
SNPshot | rs727504022 |
SNPdbe | rs727504022 |
MSV3d | rs727504022 |
GWAS Ctlg | rs727504022 |
Max Magnitude | 8.8 |
aka c.280G>A, p.Gly94Arg or G94R; mutation seen in Hispanics
ClinVar | |
---|---|
Risk | Rs727504022(A;A) |
Alt | Rs727504022(A;A) |
Reference | Rs727504022(G;G) |
Significance | Pathogenic |
Disease | not provided Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency |
Variation | info |
Gene | MUT |
CLNDBN | not provided Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency |
Reversed | 1 |
HGVS | NC_000006.11:g.49426900C>T |
CLNSRC | HGMD UniProtKB (protein) |
CLNACC | RCV000153522.2, RCV000175567.1, |