Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3
rs1437396 1.000 0.080 2 55278320 upstream gene variant C/G;T snv 3
rs1612735
ADH1B ; ADH1C
1.000 0.080 4 99336850 intron variant T/C snv 0.31 3
rs1660895 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 3
rs1693457
ADH1B
1.000 0.080 4 99315605 non coding transcript exon variant C/T snv 0.81 3
rs17028615
LOC100507053 ; ADH4
1.000 0.080 4 99150767 intron variant A/C;G snv 3
rs17125651 1.000 0.080 10 109063325 intergenic variant T/C snv 0.14 3
rs17536732
FSTL5
1.000 0.080 4 161903214 intron variant G/T snv 4.7E-02 3
rs1789891
ADH1B
1.000 0.080 4 99329262 intron variant C/A snv 0.13 3
rs181048070
LOC105374754
1.000 0.080 2 59316241 intron variant G/A snv 1.4E-02 3
rs1867877
LOC105376579 ; IGSF22
1.000 0.080 11 18705901 missense variant T/C snv 3.5E-02 4.2E-02 3
rs2002594
FAM162A
1.000 0.080 3 122392714 intron variant A/G snv 0.59 3
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 3
rs2075633
ADH1B
1.000 0.080 4 99317841 non coding transcript exon variant T/C snv 0.24 3
rs2168784 1.000 0.080 3 164872151 intergenic variant C/T snv 0.24 3
rs2173201
ADH1B
1.000 0.080 4 99329813 intron variant C/A snv 0.30 3
rs2241894
ADH1C ; ADH1B
1.000 0.080 4 99344976 synonymous variant T/A;C snv 4.0E-06; 0.30 3
rs2253612
AOX3P ; AOX3P-AOX2P
1.000 0.080 2 200703710 intron variant C/T snv 0.79 3
rs2835872
KCNJ6
1.000 0.080 21 37654970 intron variant G/A snv 0.26 3
rs34997829
LHPP
1.000 0.080 10 124546821 intron variant G/C snv 0.24 3
rs35951
ARL15
1.000 0.080 5 54296531 intron variant G/T snv 0.73 3
rs3824435
PLGRKT
1.000 0.080 9 5377115 intron variant C/G;T snv 3
rs4478858
SERINC2
1.000 0.080 1 31411078 intron variant T/C snv 0.48 3
rs4699741 1.000 0.080 4 99357540 upstream gene variant T/C snv 9.2E-02 3
rs4715221 1.000 0.080 6 51495005 regulatory region variant G/A;C;T snv 3