rs72552756
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 5 | Congenital adrenal hyperplasia |
(C;G) | 3 | Carrier of allele for congenital adrenal hyperplasia |
(G;G) | 0 | common in complete genomics |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32040692 |
Gene | CYP21A2, TNXB |
is a | snp |
is | mentioned by |
dbSNP | rs72552756 |
dbSNP (classic) | rs72552756 |
ClinGen | rs72552756 |
ebi | rs72552756 |
HLI | rs72552756 |
Exac | rs72552756 |
Gnomad | rs72552756 |
Varsome | rs72552756 |
LitVar | rs72552756 |
Map | rs72552756 |
PheGenI | rs72552756 |
Biobank | rs72552756 |
1000 genomes | rs72552756 |
hgdp | rs72552756 |
ensembl | rs72552756 |
geneview | rs72552756 |
scholar | rs72552756 |
rs72552756 | |
pharmgkb | rs72552756 |
gwascentral | rs72552756 |
openSNP | rs72552756 |
23andMe | rs72552756 |
SNPshot | rs72552756 |
SNPdbe | rs72552756 |
MSV3d | rs72552756 |
GWAS Ctlg | rs72552756 |
Max Magnitude | 5 |
ClinVar | |
---|---|
Risk | Rs72552756(C;C) |
Alt | Rs72552756(C;C) |
Reference | Rs72552756(G;G) |
Significance | Untested |
Disease | |
Variation | info |
Gene | TNXB CYP21A2 |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.32008469G>C |
CLNSRC | |
CLNACC |