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: rs17188434
rs17188434
LINC01876
2 156240264 intron variant T/C snv 4.4E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.800 1.000 1 2010 2010
dbSNP: rs1226412
rs1226412
LINC01876
1.000 0.040 2 156254801 non coding transcript exon variant C/T snv 0.73
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 2 2018 2019
dbSNP: rs72902177
rs72902177
LINC01876
2 156159745 intron variant C/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 2 2019 2019
dbSNP: rs10198345
rs10198345
LINC01876
2 156252883 intron variant T/C snv 0.38
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11883686
rs11883686
LINC01876
2 156192705 intron variant A/T snv 0.31
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs13032427
rs13032427
LINC01876
2 156070451 intron variant C/T snv 0.21
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs148043289
rs148043289
LINC01876
2 156170703 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs17244395
rs17244395
LINC01876
2 156060013 intron variant T/C snv 7.9E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs17244416
rs17244416
LINC01876
2 156060314 intron variant G/C snv 7.9E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs4538155
rs4538155
LINC01876
2 156184261 intron variant C/A;T snv
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs72902175
rs72902175
LINC01876
1.000 0.040 2 156156523 intron variant C/A;T snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2019 2019
dbSNP: rs72902177
rs72902177
LINC01876
2 156159745 intron variant C/A;T snv
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs72902177
rs72902177
LINC01876
2 156159745 intron variant C/A;T snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs72904190
rs72904190
LINC01876
2 156027428 intron variant A/G snv 7.4E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs72906060
rs72906060
LINC01876
1.000 0.040 2 156053895 intron variant T/C snv 8.4E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs72906060
rs72906060
LINC01876
1.000 0.040 2 156053895 intron variant T/C snv 8.4E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs72906064
rs72906064
LINC01876
2 156055088 intron variant G/T snv 7.9E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs7567451
rs7567451
LINC01876
1.000 0.040 2 156196868 intron variant G/T snv 0.61
CUI: C0003467
Disease: Anxiety
Anxiety 		0.700 1.000 1 2018 2018