Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10191751 1.000 0.040 2 12822189 intron variant A/G;T snv 0.68 1
rs11184959 1.000 0.040 1 106671354 intergenic variant G/A snv 0.30 1
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 1
rs12498917 1.000 0.040 4 40302730 intergenic variant A/T snv 5.0E-02 1
rs12930861 1.000 0.040 16 10492245 upstream gene variant C/A;G;T snv 1
rs139161960 1.000 0.040 5 29538059 intergenic variant T/G snv 0.10 1
rs17050244 1.000 0.040 2 120525054 regulatory region variant A/C;G snv 1
rs17073641 1.000 0.040 18 64751208 intergenic variant A/C snv 0.41 1
rs1789110 0.925 0.040 18 77147088 regulatory region variant C/A snv 0.63 1
rs2842992 0.925 0.040 6 159650127 intron variant G/A snv 0.73 1
rs4657825 1.000 0.040 1 196615191 intergenic variant A/G;T snv 1
rs4840097 1.000 0.040 6 99880322 intergenic variant C/T snv 0.64 1
rs56072732 1.000 0.040 2 236610853 intergenic variant C/T snv 5.0E-02 1
rs7517126 1.000 0.040 1 196871142 intron variant A/G snv 0.23 1
rs7519758 1.000 0.040 1 196856157 intron variant C/T snv 0.23 1
rs7676999 1.000 0.040 4 116012923 intron variant C/T snv 0.16 1
rs4932480
ABHD2
1.000 0.040 15 89180627 intron variant T/C snv 0.53 1
rs493258
ALDH1A2
0.925 0.040 15 58395681 intron variant T/C snv 0.50 1
rs920915
ALDH1A2
1.000 0.040 15 58396268 intron variant C/G snv 0.55 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs1471142
ATP6V0D1
1.000 0.040 16 67454974 non coding transcript exon variant A/G snv 4.9E-02 1
rs9542236
B3GLCT
1.000 0.040 13 31245188 intron variant T/C snv 0.34 1
rs202162020
BBS9
1.000 0.040 7 33466057 intron variant GAGA/-;GA;GAGAGA delins 2.8E-05 1
rs9380272
C2-AS1 ; CYP21A2 ; C2
1.000 0.040 6 31938233 intron variant G/A snv 1
rs1042663
C2 ; CYP21A2 ; C2-AS1
0.925 0.160 6 31937353 synonymous variant G/A snv 9.7E-02 0.12 1