rs201230446
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs201230446(C;T) |
Make rs201230446(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 72014641 |
Gene | DHODH |
is a | snp |
is | mentioned by |
dbSNP | rs201230446 |
dbSNP (classic) | rs201230446 |
ClinGen | rs201230446 |
ebi | rs201230446 |
HLI | rs201230446 |
Exac | rs201230446 |
Gnomad | rs201230446 |
Varsome | rs201230446 |
LitVar | rs201230446 |
Map | rs201230446 |
PheGenI | rs201230446 |
Biobank | rs201230446 |
1000 genomes | rs201230446 |
hgdp | rs201230446 |
ensembl | rs201230446 |
geneview | rs201230446 |
scholar | rs201230446 |
rs201230446 | |
pharmgkb | rs201230446 |
gwascentral | rs201230446 |
openSNP | rs201230446 |
23andMe | rs201230446 |
SNPshot | rs201230446 |
SNPdbe | rs201230446 |
MSV3d | rs201230446 |
GWAS Ctlg | rs201230446 |
GMAF | 0.0 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201230446(T;T) |
Alt | rs201230446(T;T) |
Reference | Rs201230446(C;C) |
Significance | Other |
Disease | Miller syndrome not provided |
Variation | info |
Gene | DHODH |
CLNDBN | Miller syndrome not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.72048540C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000018292.28, RCV000316778.1, |