Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs340874
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.830 1.000 4 2010 2019
dbSNP: rs340874
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.800 1.000 3 2010 2019
dbSNP: rs2075423
rs2075423
PROX1 ; PROX1-AS1
1.000 0.080 1 213981376 non coding transcript exon variant G/T snv 0.36
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 1 2012 2012
dbSNP: rs340874
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40
CUI: C1305855
Disease: Body mass index
Body mass index 		0.800 1.000 1 2012 2012
dbSNP: rs3767844
rs3767844
PROX1
1 214007378 intron variant A/G snv 0.35
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 2 2016 2019
dbSNP: rs340839
rs340839
PROX1 ; PROX1-AS1
1 213988477 5 prime UTR variant G/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2015 2015
dbSNP: rs366684
rs366684
PROX1
1 214013919 intron variant G/A;C snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2018 2018
dbSNP: rs366684
rs366684
PROX1
1 214013919 intron variant G/A;C snv
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2018 2018
dbSNP: rs366684
rs366684
PROX1
1 214013919 intron variant G/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3767846
rs3767846
PROX1
1 214001783 intron variant A/G snv 0.28
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs3767848
rs3767848
PROX1
1 214000497 intron variant G/A snv 0.33
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs6665764
rs6665764
PROX1
1 214004080 intron variant G/A snv 0.27
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7541039
rs7541039
PROX1
1 214003436 intron variant C/T snv 0.27
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7541039
rs7541039
PROX1
1 214003436 intron variant C/T snv 0.27
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019