Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117518788
SBF2
11 9980672 intron variant C/T snv 2.9E-02 1
rs11160546
EML1
14 99767016 intron variant C/G;T snv 1
rs17562391
HHIPL1
14 99666913 intron variant C/T snv 0.38 1
rs78350132
MEF2A
15 99660478 intron variant G/A;C;T snv 1
rs10149871
HHIPL1
14 99645618 intron variant C/T snv 0.36 1
rs4965529
MEF2A
15 99605019 intron variant C/A;T snv 1
rs2581468
MEF2A
15 99572263 intron variant C/T snv 0.65 1
rs656319 8 9956901 intergenic variant A/G snv 0.49 3
rs56243511 8 9948185 intergenic variant T/C snv 2
rs13271489 8 9946202 intergenic variant T/C snv 0.38 2
rs182770070
LZIC
1 9940418 intron variant A/T snv 5.8E-03 2
rs1257310 14 99344090 intergenic variant C/A snv 0.81 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs8022678 14 98900353 intergenic variant A/C;G snv 2
rs62491354 8 9873153 intergenic variant G/A snv 0.13 1
rs187821766
STK3
8 98729050 intron variant C/T snv 3.5E-03 3
rs1871190 5 98618015 intergenic variant G/T snv 0.28 1
rs186208701
STK3
8 98567888 intron variant T/C snv 3.3E-03 3
rs4841235 8 9825848 intergenic variant A/G snv 0.56 2
rs1976671 8 9822124 intergenic variant A/C;G;T snv 2
rs8009025
LOC105370655
14 98164834 intron variant T/C snv 0.19 1
rs10147464
LOC105370655
14 98122398 intron variant A/G;T snv 1
rs11599481
CRTAC1
10 97880706 intron variant C/T snv 0.19 2
rs9374896 6 97862608 intron variant C/G;T snv 1
rs902621
LINC00923
15 97801833 intron variant T/C snv 0.24 1