Source: CURATED

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: rs1079596
rs1079596
11 113425897 intron variant C/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs11214606
rs11214606
11 113439147 intron variant C/T snv 3.4E-02
CUI: C0025265
Disease: Memory, Short-Term
Memory, Short-Term
0.700 1.000 1 2011 2011
dbSNP: rs11214607
rs11214607
1.000 0.040 11 113441417 intron variant T/G snv 0.16
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2018 2018
dbSNP: rs11214607
rs11214607
1.000 0.040 11 113441417 intron variant T/G snv 0.16
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
0.700 1.000 1 2018 2018
dbSNP: rs17601612
rs17601612
11 113447023 intron variant G/C snv 0.27
CUI: C0424574
Disease: Duration of sleep
Duration of sleep
0.700 1.000 1 2017 2017
dbSNP: rs2734839
rs2734839
1.000 0.040 11 113415768 intron variant C/A;T snv
CUI: C0582591
Disease: Processing speed
Processing speed
0.700 1.000 1 2016 2016
dbSNP: rs7131440
rs7131440
11 113429188 intron variant C/T snv 0.44
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs7131627
rs7131627
11 113429107 intron variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018