Tag
Steroid Metabolism
15 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs104894085 | STAR Q258X (c.772C>T) | Nonsense mutation in STAR that abolishes steroidogenic acute regulatory prote... | Reproductive Hormones | Established | |
| rs104894135 | CYP17A1 Ser106Pro | Pathogenic missense variant in CYP17A1 causing complete loss of 17α-hydroxyla... | Reproductive Hormones | Established | |
| rs104894136 | CYP17A1 Arg239* | Pathogenic nonsense variant in CYP17A1 introducing a premature stop codon at ... | Reproductive Hormones | Established | |
| rs1052373 | MYBPC3 | Cardiac myosin-binding protein variant strongly associated with endurance ath... | Fitness & Body | Strong | |
| rs104894137 | CYP17A1 Pro342Thr | Missense variant in CYP17A1 reducing both 17α-hydroxylase and 17,20-lyase act... | Reproductive Hormones | Strong | |
| rs104894141 | CYP17A1 W17X | Rare pathogenic nonsense variant in CYP17A1 causing complete abolition of 17α... | Reproductive Hormones | Established | |
| rs1799998 | CYP11B2 -344C>T | Promoter variant in aldosterone synthase increasing CYP11B2 transcription, as... | Blood Pressure & Hypertension | Moderate | |
| rs137852690 | STAR A218V | STAR missense variant abolishing steroidogenic activity; homozygous carriers ... | Reproductive Hormones | Established | |
| rs2268797 | SRD5A2 SRD5A2 intronic variant | Intronic variant in SRD5A2 tagging haplotype backgrounds that differ in 5-alp... | Reproductive Hormones | Emerging | |
| rs28934880 | HSD3B2 Ala10Glu | Missense variant abolishing 3β-hydroxysteroid dehydrogenase type 2 activity; ... | Reproductive Hormones | Strong | |
| rs6162 | CYP17A1 His46= | Synonymous coding variant in CYP17A1 that tags a haplotype linked to altered ... | Reproductive Hormones | Moderate | |
| rs7594951 | SRD5A2 SRD5A2 intron 4 regulatory variant | Deep intronic variant in the testosterone-to-DHT converting enzyme; the minor... | Reproductive Hormones | Emerging | |
| rs760695410 | CYP17A1 p.His373Leu | Pathogenic missense variant in CYP17A1 disrupting the heme-binding region of ... | Reproductive Hormones | Established | |
| rs28936701 | CYP1B1 R469W | Pathogenic CYP1B1 missense variant (Arg469Trp) that severely reduces enzyme a... | Vascular Inflammation & Remodeling | Established | |
| rs80358216 | HSD3B2 Trp171X | Pathogenic nonsense variant introducing a premature stop codon at position 17... | Reproductive Hormones | Established |