rs10418
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs10418(C;T) |
Make rs10418(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 30626965 |
Gene | TCN2 |
is a | snp |
is | mentioned by |
dbSNP | rs10418 |
dbSNP (classic) | rs10418 |
ClinGen | rs10418 |
ebi | rs10418 |
HLI | rs10418 |
Exac | rs10418 |
Gnomad | rs10418 |
Varsome | rs10418 |
LitVar | rs10418 |
Map | rs10418 |
PheGenI | rs10418 |
Biobank | rs10418 |
1000 genomes | rs10418 |
hgdp | rs10418 |
ensembl | rs10418 |
geneview | rs10418 |
scholar | rs10418 |
rs10418 | |
pharmgkb | rs10418 |
gwascentral | rs10418 |
openSNP | rs10418 |
23andMe | rs10418 |
SNPshot | rs10418 |
SNPdbe | rs10418 |
MSV3d | rs10418 |
GWAS Ctlg | rs10418 |
GMAF | 0.2571 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23089108] Idiopathic pulmonary fibrosis and polymorphisms of the folate pathway genes
ClinVar | |
---|---|
Risk | rs10418(T;T) |
Alt | rs10418(T;T) |
Reference | Rs10418(C;C) |
Significance | Non-pathogenic |
Disease | Transcobalamin II deficiency |
Variation | info |
Gene | TCN2 |
CLNDBN | Transcobalamin II deficiency |
Reversed | 0 |
HGVS | NC_000022.10:g.31022952C>T |
CLNSRC | |
CLNACC | RCV000339325.1, |