Source: ALL

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: rs10798879
rs10798879
HCRTR1 ; PEF1
1 31631214 intron variant T/C snv 0.55
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs10798880
rs10798880
HCRTR1 ; PEF1
1 31631487 intron variant G/A;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2017 2017
dbSNP: rs10798882
rs10798882
PEF1 ; PEF1-AS1
1 31642946 intron variant C/G snv 0.58
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2017 2017
dbSNP: rs4949454
rs4949454
PEF1
1 31633440 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs7546297
rs7546297
PEF1
1 31640893 intron variant A/G snv 0.54
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018