Gene: TOMM40 ×
Source: GWASDB ×
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
20 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.800 1.000 3 2009 2013
dbSNP: rs1160985
rs1160985
TOMM40
5 1.000 0.080 19 44900155 intron variant C/T snv 0.52 0.800 1.000 1 2013 2019
dbSNP: rs157580
rs157580
TOMM40
11 0.882 0.160 19 44892009 intron variant G/A snv 0.69 0.700 1.000 1 2012 2012
dbSNP: rs76366838
rs76366838
TOMM40
1 19 44896639 intron variant G/A;T snv 0.700 1.000 1 2012 2012