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: rs2252074
rs2252074
KMT2E ; LINC01004
7 104953806 non coding transcript exon variant T/G snv 0.43
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs34180096
rs34180096
KMT2E ; LINC01004
7 104968145 intron variant T/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs56016333
rs56016333
KMT2E ; LINC01004
7 104955801 intron variant T/C snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs56016333
rs56016333
KMT2E ; LINC01004
7 104955801 intron variant T/C snv 0.30
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7776707
rs7776707
KMT2E ; LINC01004
1.000 0.040 7 104965083 intron variant C/A snv 0.31
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs7776707
rs7776707
KMT2E ; LINC01004
1.000 0.040 7 104965083 intron variant C/A snv 0.31
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019