CYP17A1
From SNPedia
is a | gene |
is | mentioned by |
Full name | cytochrome P450, family 17, subfamily A, polypeptide 1 |
EntrezGene | 1586 |
PheGenI | 1586 |
VariationViewer | 1586 |
ClinVar | CYP17A1 |
GeneCards | CYP17A1 |
dbSNP | 1586 |
Diseases | CYP17A1 |
SADR | 1586 |
HugeNav | 1586 |
CYPANC | cyp17a1 |
wikipedia | CYP17A1 |
CYP17A1 | |
gopubmed | CYP17A1 |
EVS | CYP17A1 |
HEFalMp | CYP17A1 |
MyGene2 | CYP17A1 |
23andMe | CYP17A1 |
UniProt | P05093 |
Ensembl | ENSG00000148795 |
OMIM | 609300 |
# SNPs | 43 |
Max Magnitude | Chromosome position | Summary | |
---|---|---|---|
i5001477 | |||
i5001478 | |||
i5001486 | |||
i5001487 | |||
i5001488 | |||
i5001490 | |||
i5001492 | |||
i5001495 | |||
rs1004467 | 0 | 102,834,750 | |
rs104894135 | 6.6 | 102,835,374 | |
rs104894136 | 0 | 102,834,074 | |
rs104894137 | 6.3 | 102,832,626 | |
rs104894138 | 6.6 | 102,837,076 | |
rs104894139 | 3 | 102,832,577 | |
rs104894141 | 6.6 | 102,837,311 | |
rs104894142 | 6.6 | 102,832,566 | |
rs104894143 | 6.6 | 102,831,535 | |
rs104894144 | 6.6 | 102,832,665 | |
rs104894145 | 6.6 | 102,830,946 | |
rs104894146 | 6.6 | 102,837,084 | |
rs104894147 | 6.6 | 102,835,350 | |
rs104894148 | 6.3 | 102,835,343 | |
rs104894149 | 6.3 | 102,832,611 | |
rs104894150 | 6.3 | 102,834,850 | |
rs104894151 | 6.3 | 102,830,871 | |
rs104894152 | 6.6 | 102,837,281 | |
rs104894153 | 6.6 | 102,837,075 | |
rs104894154 | 6.6 | 102,835,316 | |
rs104894155 | 6.6 | 102,830,982 | |
rs1060499582 | 0 | 102,831,589 | |
rs10883783 | 0 | 102,831,395 | |
rs121434319 | 6.3 | 102,837,203 | |
rs17115100 | 2 | 102,831,636 | |
rs17115149 | 0 | 102,837,961 | |
rs2486758 | 2.2 | 102,837,723 | |
rs3781287 | 0 | 102,835,663 | |
rs3824755 | 0 | 102,836,092 | |
rs556794126 | 0 | 102,830,790 | |
rs6162 | 0 | 102,837,224 | |
rs61754278 | 0 | 102,832,610 | |
rs743572 | 0 | 102,837,395 | |
rs786205061 | 6.6 | 102,835,249 | |
rs786205062 | 6.3 | 102,837,132 |
The CYP17A1 gene encodes steroid 17-alpha-hydroxylase, also referred to as steroid 17-alpha-monooxygenase. Mutations in the CYP17A1 gene are primary linked to forms of 17-alpha-hydroxylase/17,20-lyase deficiency related disorders, but risk factors for other conditions have also been reported for some SNPs.