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Table 2 Characteristics of polymorphisms associated with POI in which were included in this study

From: Micronutrients intake and genetic variants associated with premature ovarian insufficiency; MASHAD cohort study

SNP

Gene

Alleles

Chromosome

MAF (1000Genomes)

Method genotyping

Ref

rs4806660

TMEM

T > C

19:55313266

C = 0.330

ASO

[32,33,34]

rs451417

MCM8

C > A

20:5961353

A = 0.280

ASO

[35]

rs16991615

MCM8

G > A

20:5967581

A = 0.026

ASO

[36, 37, 32]

rs7246479

BRSK1

T > A

19:55312964

T = 0.410

ASO

[15, 38, 39]

rs244715

ZNF346

A > G

5:177076562

A = 0.380

ASO

[39, 34]

rs1046089

PRRC2A

G > A

6:31635190

A = 0.390

ASO

[40,41,42]

rs2303369

FNDC4

C > T

2:27492549

T = 0.350

ASO

[43, 44]

rs10183486

TLK1

C > T

2:171134461

T = 0.310

Tetra ARMS

[43, 45]

  1. POI: premature ovarian insufficiency; SNP: Single nucleotide polymorphism