rs200491579
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs200491579(C;T) |
Make rs200491579(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 14 |
Position | 24261826 |
Gene | TGM1 |
is a | snp |
is | mentioned by |
dbSNP | rs200491579 |
dbSNP (classic) | rs200491579 |
ClinGen | rs200491579 |
ebi | rs200491579 |
HLI | rs200491579 |
Exac | rs200491579 |
Gnomad | rs200491579 |
Varsome | rs200491579 |
LitVar | rs200491579 |
Map | rs200491579 |
PheGenI | rs200491579 |
Biobank | rs200491579 |
1000 genomes | rs200491579 |
hgdp | rs200491579 |
ensembl | rs200491579 |
geneview | rs200491579 |
scholar | rs200491579 |
rs200491579 | |
pharmgkb | rs200491579 |
gwascentral | rs200491579 |
openSNP | rs200491579 |
23andMe | rs200491579 |
SNPshot | rs200491579 |
SNPdbe | rs200491579 |
MSV3d | rs200491579 |
GWAS Ctlg | rs200491579 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200491579(T;T) |
Alt | rs200491579(T;T) |
Reference | Rs200491579(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TGM1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000014.8:g.24731032C>T |
CLNSRC | |
CLNACC | RCV000329115.1, |