rs147277149
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs147277149(C;T) |
Make rs147277149(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 5 |
Position | 7895749 |
Gene | MTRR |
is a | snp |
is | mentioned by |
dbSNP | rs147277149 |
dbSNP (classic) | rs147277149 |
ClinGen | rs147277149 |
ebi | rs147277149 |
HLI | rs147277149 |
Exac | rs147277149 |
Gnomad | rs147277149 |
Varsome | rs147277149 |
LitVar | rs147277149 |
Map | rs147277149 |
PheGenI | rs147277149 |
Biobank | rs147277149 |
1000 genomes | rs147277149 |
hgdp | rs147277149 |
ensembl | rs147277149 |
geneview | rs147277149 |
scholar | rs147277149 |
rs147277149 | |
pharmgkb | rs147277149 |
gwascentral | rs147277149 |
openSNP | rs147277149 |
23andMe | rs147277149 |
SNPshot | rs147277149 |
SNPdbe | rs147277149 |
MSV3d | rs147277149 |
GWAS Ctlg | rs147277149 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs147277149(T;T) |
Alt | rs147277149(T;T) |
Reference | Rs147277149(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | MTRR |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.7895862C>T |
CLNSRC | |
CLNACC | RCV000254795.1, |