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: rs7590342
rs7590342
LINC01122
2 59033269 intron variant A/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs77732866
rs77732866
LINC01122
2 58752744 intron variant G/A snv 0.11
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs929641
rs929641
LINC01122
2 58565242 intron variant A/G snv 0.45
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.700 1.000 1 2015 2015
dbSNP: rs10175478
rs10175478
LINC01122
0.925 0.040 2 58913731 intron variant C/A;T snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs10175478
rs10175478
LINC01122
0.925 0.040 2 58913731 intron variant C/A;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs13417036
rs13417036
LINC01122
1.000 0.080 2 58694642 intron variant G/A snv 0.16
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2019 2019
dbSNP: rs2215939
rs2215939
LINC01122
1.000 0.040 2 58492312 intron variant T/A snv 0.57
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs2215939
rs2215939
LINC01122
1.000 0.040 2 58492312 intron variant T/A snv 0.57
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs2708146
rs2708146
LINC01122
1.000 0.120 2 58728818 intron variant A/G snv 0.47
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome 		0.710 1.000 1 2019 2019
dbSNP: rs35609938
rs35609938
LINC01122
1.000 0.040 2 58529594 intron variant T/C snv 0.37
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs35609938
rs35609938
LINC01122
1.000 0.040 2 58529594 intron variant T/C snv 0.37
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs6731302
rs6731302
LINC01122
1.000 0.080 2 58606358 intron variant A/G;T snv
CUI: C0028754
Disease: Obesity
Obesity 		0.800 1.000 1 2013 2013
dbSNP: rs6731302
rs6731302
LINC01122
1.000 0.080 2 58606358 intron variant A/G;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019