Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6729965 2 232353552 upstream gene variant T/C snv 0.22 2
rs11648166 16 58662802 downstream gene variant A/G snv 0.12 1
rs12149056 16 58657060 intergenic variant T/A snv 0.12 1
rs28845026 2 232355544 upstream gene variant C/A;G;T snv 1
rs55738617 2 232352849 upstream gene variant C/T snv 0.22 1
rs60979655 16 58661235 downstream gene variant C/T snv 0.12 1
rs6715083 2 232353782 upstream gene variant C/T snv 0.22 1
rs6715187 2 232353879 upstream gene variant C/A;G;T snv 1
rs6715387 2 232353864 upstream gene variant G/A snv 0.22 1
rs4996188
ECEL1P3
2 232350750 intron variant C/T snv 0.22 1
rs883013
ECEL1P3
2 232350693 intron variant C/T snv 0.22 1
rs1065643
MTA3 ; HAAO
2 42794053 upstream gene variant T/C snv 0.14 1
rs11639682
SLC38A7
16 58673228 intron variant C/A snv 0.14 1
rs12598355
SLC38A7
16 58669872 intron variant G/C snv 0.13 1
rs16960359
SLC38A7
16 58670592 intron variant G/A;C snv 1
rs3784911
SLC38A7
16 58669712 intron variant C/T snv 0.12 1
rs76733922
SLC38A7
16 58668637 intron variant G/A;C snv 1
rs75690380
SVIL
10 29647954 intron variant T/A;G snv 1
rs77628230
SVIL
10 29653623 intron variant A/C;T snv 1
rs80082057
SVIL
10 29652692 intron variant C/T snv 4.0E-02 1