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: rs6651252
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 5 2010 2019
dbSNP: rs1516971
rs1516971
LINC00824
1.000 0.120 8 128529854 intron variant T/C snv 0.19
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 2 2014 2019
dbSNP: rs1561927
rs1561927
LINC00824
0.807 0.280 8 128555832 intron variant C/T snv 0.65
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 1 2014 2014
dbSNP: rs7815944
rs7815944
LINC00824
1.000 0.120 8 128415272 intron variant A/G snv 0.12
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.800 1.000 1 2012 2012
dbSNP: rs10088218
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.710 1.000 2 2010 2013
dbSNP: rs1561927
rs1561927
LINC00824
0.807 0.280 8 128555832 intron variant C/T snv 0.65
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.710 1.000 2 2014 2019
dbSNP: rs6651252
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 2 2015 2017
dbSNP: rs10088218
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer 		0.700 1.000 1 2015 2015
dbSNP: rs11785816
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs11785816
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs11785816
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs11785816
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs1400482
rs1400482
LINC00824
0.925 0.120 8 128529685 intron variant G/A snv 0.13
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs1400482
rs1400482
LINC00824
0.925 0.120 8 128529685 intron variant G/A snv 0.13
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2017 2017
dbSNP: rs1561924
rs1561924
LINC00824
1.000 0.040 8 128557125 intron variant G/A snv 0.18
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019
dbSNP: rs17232730
rs17232730
LINC00824
1.000 0.080 8 128525500 intron variant G/C snv 9.8E-02
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs17804358
rs17804358
LINC00824
8 128439451 intron variant C/T snv 0.48
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs35286446
rs35286446
LINC00824
1.000 0.080 8 128433618 intron variant TATATA/-;TATA;TATATATA;TATATATATA delins
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs4598218
rs4598218
LINC00824
8 128471710 intron variant C/T snv 0.48
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs6651252
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2016 2016
dbSNP: rs6651252
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs6651252
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs6651252
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs6651252
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs6651252
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2016 2016