rs146075796
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs146075796(C;T) |
Make rs146075796(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 6 |
Position | 39909834 |
Gene | MOCS1 |
is a | snp |
is | mentioned by |
dbSNP | rs146075796 |
dbSNP (classic) | rs146075796 |
ClinGen | rs146075796 |
ebi | rs146075796 |
HLI | rs146075796 |
Exac | rs146075796 |
Gnomad | rs146075796 |
Varsome | rs146075796 |
LitVar | rs146075796 |
Map | rs146075796 |
PheGenI | rs146075796 |
Biobank | rs146075796 |
1000 genomes | rs146075796 |
hgdp | rs146075796 |
ensembl | rs146075796 |
geneview | rs146075796 |
scholar | rs146075796 |
rs146075796 | |
pharmgkb | rs146075796 |
gwascentral | rs146075796 |
openSNP | rs146075796 |
23andMe | rs146075796 |
SNPshot | rs146075796 |
SNPdbe | rs146075796 |
MSV3d | rs146075796 |
GWAS Ctlg | rs146075796 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs146075796(T;T) |
Alt | rs146075796(T;T) |
Reference | Rs146075796(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MOCS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.39877578C>T |
CLNSRC | |
CLNACC | RCV000254772.1, |