rs148579886
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs148579886(A;A) |
Make rs148579886(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 39909922 |
Gene | MOCS1 |
is a | snp |
is | mentioned by |
dbSNP | rs148579886 |
dbSNP (classic) | rs148579886 |
ClinGen | rs148579886 |
ebi | rs148579886 |
HLI | rs148579886 |
Exac | rs148579886 |
Gnomad | rs148579886 |
Varsome | rs148579886 |
LitVar | rs148579886 |
Map | rs148579886 |
PheGenI | rs148579886 |
Biobank | rs148579886 |
1000 genomes | rs148579886 |
hgdp | rs148579886 |
ensembl | rs148579886 |
geneview | rs148579886 |
scholar | rs148579886 |
rs148579886 | |
pharmgkb | rs148579886 |
gwascentral | rs148579886 |
openSNP | rs148579886 |
23andMe | rs148579886 |
SNPshot | rs148579886 |
SNPdbe | rs148579886 |
MSV3d | rs148579886 |
GWAS Ctlg | rs148579886 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs148579886(A;A) |
Alt | rs148579886(A;A) |
Reference | Rs148579886(G;G) |
Significance | Probable-non-pathogenic |
Disease | Molybdenum cofactor deficiency not provided |
Variation | info |
Gene | MOCS1 |
CLNDBN | Molybdenum cofactor deficiency, complementation group A not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.39877666G>A |
CLNSRC | |
CLNACC | RCV000190510.2, RCV000416188.1, |