Table 2.
S no | Gene | Cytogenic location | Anomalies | Author | Reference |
---|---|---|---|---|---|
1 | AR | Xq12 | X inactivation | Urbanek | [23] |
2 | FSHR | 2p16.3 | Gene variation | Aesha Sh | [25]. |
3 | FTO | 16q12.2 | SNP rs9939609 | Rizwan S | (Rizwan S, 2018) |
4 | CAPN10 | 2q37.3 | Polymorphism | Margrit Urbanek | [29] |
5 | CYPA1A | 15q24.1 | T6235C | K Arvind Babu | [33] |
6 | CYP11A1 | 15q24.1 | SNP rs4077582 | Cheng-wei zhang | [36]. |
7 | CYP17A1 | 10q24.32 | T > C | Li Li | [41]. |
8 | CYP1A1 | 15q24.1 | Ile/Val | Ibrahim Esinler | [32]. |
9 | CYP21A2 | 6p21.33 | Heterozygous mutation | Settas N | [44]. |
10 | CYP3A7 | 7q22.1 | Variant allele | Mark O goodarzi | [46] |
11 | CYP19A1 | 15q21.2 | Arg264Cys | K Ranjith reddy | [6]. |