Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2075650
rs2075650
TOMM40
12 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.800 1.000 1 2014 2014
dbSNP: rs115881343
rs115881343
TOMM40
1 1.000 0.040 19 44899959 intron variant C/G;T snv 2.9E-02 0.710 1.000 1 2014 2014
dbSNP: rs429358
rs429358
APOE
26 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.710 1.000 1 2017 2019
dbSNP: rs769449
rs769449
APOE
8 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 0.710 1.000 1 2014 2014
dbSNP: rs10073892
rs10073892
SLCO6A1
1 5 102391066 non coding transcript exon variant T/C snv 0.24 0.21 0.700 1.000 1 2014 2014
dbSNP: rs16885997
rs16885997 		1 8 114496877 intergenic variant G/T snv 3.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs17641411
rs17641411
GABRA4
1 4 46941670 intron variant C/T snv 2.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs73643144
rs73643144
TEK
1 9 27126454 intron variant T/C snv 3.5E-02 0.700 1.000 1 2017 2017