rs568165874
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs568165874(C;T) |
Make rs568165874(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 12 |
Position | 57763738 |
Gene | CYP27B1 |
is a | snp |
is | mentioned by |
dbSNP | rs568165874 |
dbSNP (classic) | rs568165874 |
ClinGen | rs568165874 |
ebi | rs568165874 |
HLI | rs568165874 |
Exac | rs568165874 |
Gnomad | rs568165874 |
Varsome | rs568165874 |
LitVar | rs568165874 |
Map | rs568165874 |
PheGenI | rs568165874 |
Biobank | rs568165874 |
1000 genomes | rs568165874 |
hgdp | rs568165874 |
ensembl | rs568165874 |
geneview | rs568165874 |
scholar | rs568165874 |
rs568165874 | |
pharmgkb | rs568165874 |
gwascentral | rs568165874 |
openSNP | rs568165874 |
23andMe | rs568165874 |
SNPshot | rs568165874 |
SNPdbe | rs568165874 |
MSV3d | rs568165874 |
GWAS Ctlg | rs568165874 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs568165874(G;G) rs568165874(T;T) |
Alt | rs568165874(G;G) rs568165874(T;T) |
Reference | Rs568165874(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CYP27B1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.58157521C>G |
CLNSRC | |
CLNACC | RCV000255484.1, |