rs121964979
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 3 | Carrier of a glycine encephalopathy mutation |
(T;T) | 8.8 | Glycine encephalopathy; Non-ketotic hyperglycinemia |
Reference | GRCh37 37.1/132 |
Chromosome | 9 |
Position | 6595109 |
Gene | GLDC |
is a | snp |
is | mentioned by |
dbSNP | rs121964979 |
dbSNP (classic) | rs121964979 |
ClinGen | rs121964979 |
ebi | rs121964979 |
HLI | rs121964979 |
Exac | rs121964979 |
Gnomad | rs121964979 |
Varsome | rs121964979 |
LitVar | rs121964979 |
Map | rs121964979 |
PheGenI | rs121964979 |
Biobank | rs121964979 |
1000 genomes | rs121964979 |
hgdp | rs121964979 |
ensembl | rs121964979 |
geneview | rs121964979 |
scholar | rs121964979 |
rs121964979 | |
pharmgkb | rs121964979 |
gwascentral | rs121964979 |
openSNP | rs121964979 |
23andMe | rs121964979 |
SNPshot | rs121964979 |
SNPdbe | rs121964979 |
MSV3d | rs121964979 |
GWAS Ctlg | rs121964979 |
Max Magnitude | 8.8 |
c.1166C>T (p.Ala389Val)
23andMe calls this i5007986
ClinVar | |
---|---|
Risk | Rs121964979(T;T) |
Alt | Rs121964979(T;T) |
Reference | Rs121964979(C;C) |
Significance | Pathogenic |
Disease | Non-ketotic hyperglycinemia not provided |
Variation | info |
Gene | GLDC |
CLNDBN | Non-ketotic hyperglycinemia not provided |
Reversed | 1 |
HGVS | NC_000009.11:g.6595109G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000012769.17, RCV000482511.1, |