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: rs3130783
rs3130783
LINC00243
1.000 0.040 6 30806580 intron variant G/A;T snv
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.810 1.000 1 2013 2019
dbSNP: rs886424
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.800 1.000 1 2007 2015
dbSNP: rs886424
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.710 1.000 1 2012 2012
dbSNP: rs114964506
rs114964506
LINC00243
1.000 0.040 6 30814428 non coding transcript exon variant G/C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs114964506
rs114964506
LINC00243
1.000 0.040 6 30814428 non coding transcript exon variant G/C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs115915654
rs115915654
LINC00243
1.000 0.040 6 30801949 intron variant C/T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs115915654
rs115915654
LINC00243
1.000 0.040 6 30801949 intron variant C/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs116396069
rs116396069
LINC00243
1.000 0.040 6 30830920 upstream gene variant C/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs1264347
rs1264347
LINC00243
1.000 0.040 6 30830920 upstream gene variant C/T snv 7.9E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs1264347
rs1264347
LINC00243
1.000 0.040 6 30830920 upstream gene variant C/T snv 7.9E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs1264347
rs1264347
LINC00243
1.000 0.040 6 30830920 upstream gene variant C/T snv 7.9E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2019 2019
dbSNP: rs1264347
rs1264347
LINC00243
1.000 0.040 6 30830920 upstream gene variant C/T snv 7.9E-02
CUI: C0011847
Disease: Diabetes
Diabetes 		0.700 1.000 1 2019 2019
dbSNP: rs1264351
rs1264351
LINC00243
6 30824340 intron variant G/C snv 7.8E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs151302046
rs151302046
LINC00243
6 30807354 intron variant G/A;C snv
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement 		0.700 1.000 1 2019 2019
dbSNP: rs4587207
rs4587207
LINC00243
1.000 6 30799168 intron variant A/G snv 0.17
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2015 2015
dbSNP: rs4713376
rs4713376
LINC00243
1.000 0.080 6 30805537 intron variant A/C snv 0.12
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		0.700 1.000 1 2019 2019
dbSNP: rs886424
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2012 2012
dbSNP: rs886424
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2015 2015