Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1156737044
rs1156737044
C 0.800 GeneticVariation CLINVAR Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest. 28965849

2017

dbSNP: rs1361024832
rs1361024832
T 0.800 GeneticVariation CLINVAR Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest. 28965849

2017

dbSNP: rs1156737044
rs1156737044
0.800 GeneticVariation UNIPROT

dbSNP: rs1361024832
rs1361024832
0.800 GeneticVariation UNIPROT

dbSNP: rs1351320025
rs1351320025
A 0.700 GeneticVariation CLINVAR Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest. 28965849

2017

dbSNP: rs1397500378
rs1397500378
0.700 GeneticVariation UNIPROT Female Infertility Caused by Mutations in the Oocyte-Specific Translational Repressor PATL2. 28965844

2017

dbSNP: rs1397500378
rs1397500378
0.700 GeneticVariation UNIPROT Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest. 28965849

2017

dbSNP: rs548527219
rs548527219
A 0.700 GeneticVariation CLINVAR Female Infertility Caused by Mutations in the Oocyte-Specific Translational Repressor PATL2. 28965844

2017

dbSNP: rs569729547
rs569729547
0.700 GeneticVariation UNIPROT Female Infertility Caused by Mutations in the Oocyte-Specific Translational Repressor PATL2. 28965844

2017

dbSNP: rs569729547
rs569729547
0.700 GeneticVariation UNIPROT Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest. 28965849

2017

dbSNP: rs752734259
rs752734259
T 0.700 CausalMutation CLINVAR Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest. 28965849

2017

dbSNP: rs1011539285
rs1011539285
0.700 GeneticVariation UNIPROT

dbSNP: rs1351320025
rs1351320025
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555385717
rs1555385717
G 0.700 CausalMutation CLINVAR

dbSNP: rs548527219
rs548527219
A 0.700 CausalMutation CLINVAR