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Table 1 Genes with a significant presence of SNVs in patients with ovarian failure

From: Whole-exome sequencing and Drosophila modelling reveal mutated genes and pathways contributing to human ovarian failure

Gene symbol

Position in genome

Nº SNV

Adjusted p-value

CDC27

17:47117703–47,189,422

9

5.35E-55

ANKRD20A1

9:67832765–67,920,552

2

5.35E-55

IGSF3

1:116574399–116,667,755

1

3.64E-54

KMT5A

12:123384132–123,409,353

1

5.36E-53

FAM104B

X:55,143,102–55,161,310

2

1.08E-38

KMT2C

7:152134922–152,436,644

4

5.09E-33

MTCH2

11:47617315–47,642,607

5

1.48E-25

CTBP2

10:124984317–125,161,170

20

1.12E-24

AK2

1:33007940–33,080,996

2

1.54E-19

ANKRD36B

2:97492663–97,589,877

1

7.02E-17

WDR89

14:63597039–63,641,871

4

1.60E-11

ESRRA

11:64305497–64,316,743

2

2.43E-08

MST1

3:49683947–49,689,501

2

1.68E-07

ZNF717

3:75678660–75,785,583

9

3.59E-07

TEKT4

2:94871430–94,876,823

1

4.18E-03

CFTR

7:117287120–117,715,971

4

5.75E-03

HLA-DRB1

6:32578769–32,589,848

1

1.30E-02

MLH1

3:36993350–37,050,846

2

2.51E-02