PROX1-AS1, PROX1 antisense RNA 1, 100505832

N. diseases: 9; N. variants: 8
Source: GWASCAT ×
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs340874
rs340874
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.830 1.000 4 2010 2019
dbSNP: rs340874
rs340874
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
1.000 0.080 1 213981376 non coding transcript exon variant G/T snv 0.36
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs340874
rs340874
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: rs4342822
rs4342822
0.882 0.080 1 213850882 intron variant G/T snv 0.62
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.710 1.000 1 2017 2017
dbSNP: rs7529073
rs7529073
1.000 0.040 1 213974546 intron variant T/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 3 2015 2019
dbSNP: rs115732928
rs115732928
1.000 0.040 1 213980745 intron variant A/T snv 3.6E-02
CUI: C0004106
Disease: Astigmatism
Astigmatism
Eye Diseases 0.700 1.000 1 2018 2018
dbSNP: rs182234674
rs182234674
1 213932400 intron variant G/T snv 1.4E-05
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
0.700 1.000 1 2015 2015
dbSNP: rs340839
rs340839
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: rs4342822
rs4342822
0.882 0.080 1 213850882 intron variant G/T snv 0.62
CUI: C0278704
Disease: Malignant Childhood Neoplasm
Malignant Childhood Neoplasm
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs79687284
rs79687284
1 213977478 intron variant G/A;C;T snv
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.700 1.000 1 2017 2017