Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2246434
SPTA1
1 158648665 intron variant G/A snv 0.26 0.22 2
rs2340727 1 161976937 intergenic variant A/G snv 0.33 2
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 2
rs4657616
IFI16 ; PYDC5
1 159001296 intron variant A/G snv 0.31 2
rs12135894 1 3811497 downstream gene variant C/A;T snv 1
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 1
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 1
rs7529925
LINC01221
1 199038079 intron variant C/T snv 0.77 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs13027161
MIR4432HG
2 60380593 intron variant T/C snv 0.29 3
rs2540917
MIR4432HG
2 60381624 intron variant T/C snv 0.29 3
rs10207392
ACOXL ; MIR4435-2HG
2 111092082 intron variant A/G snv 0.48 1
rs243070
MIR4432HG
2 60393151 intron variant T/A snv 0.21 1
rs6729815
BCL11A
1.000 0.080 2 60496537 intron variant T/C snv 0.49 1
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 2
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 2
rs9310736
THRB
3 24309320 intron variant A/G snv 0.69 2
rs9859260
TFRC
3 196073676 intron variant C/A;T snv 2
rs12490148
LOC105374116 ; SRPRB
3 133805129 non coding transcript exon variant C/T snv 0.29 1
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 1
rs3893275
LOC105374303
3 196192085 regulatory region variant A/C snv 0.13 1
rs4916483 3 196180782 intergenic variant T/C snv 0.12 1
rs6776003
RASA2
1.000 0.080 3 141547651 intron variant G/A snv 0.55 1
rs7615316
PLS1 ; LOC105374136
3 142637084 intron variant G/A snv 0.61 1
rs9683085
ATR
3 142529656 intron variant G/A snv 0.64 1