rs72552757
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
(C;T) | 3 | Carrier of allele for congenital adrenal hyperplasia |
(T;T) | 5 | Congenital adrenal hyperplasia |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32040871 |
Gene | CYP21A2, TNXB |
is a | snp |
is | mentioned by |
dbSNP | rs72552757 |
dbSNP (classic) | rs72552757 |
ClinGen | rs72552757 |
ebi | rs72552757 |
HLI | rs72552757 |
Exac | rs72552757 |
Gnomad | rs72552757 |
Varsome | rs72552757 |
LitVar | rs72552757 |
Map | rs72552757 |
PheGenI | rs72552757 |
Biobank | rs72552757 |
1000 genomes | rs72552757 |
hgdp | rs72552757 |
ensembl | rs72552757 |
geneview | rs72552757 |
scholar | rs72552757 |
rs72552757 | |
pharmgkb | rs72552757 |
gwascentral | rs72552757 |
openSNP | rs72552757 |
23andMe | rs72552757 |
SNPshot | rs72552757 |
SNPdbe | rs72552757 |
MSV3d | rs72552757 |
GWAS Ctlg | rs72552757 |
Max Magnitude | 5 |
ClinVar | |
---|---|
Risk | Rs72552757(T;T) |
Alt | Rs72552757(T;T) |
Reference | Rs72552757(C;C) |
Significance | Untested |
Disease | |
Variation | info |
Gene | TNXB CYP21A2 |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000006.11:g.32008648C>T |
CLNSRC | |
CLNACC |