Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77936863
CD300LF ; RAB37
17 74700954 intron variant A/- del 0.54 1
rs6500550
TRAP1
16 3696240 intron variant C/G;T snv 5
rs305082
IRF8
16 85903372 non coding transcript exon variant T/C snv 0.28 3
rs60606273 15 64362768 intron variant A/T snv 0.84 5
rs2250635
EHD4
15 41969267 intron variant T/C snv 0.18 4
rs3131610
USP50 ; USP8
15 50507898 3 prime UTR variant G/A snv 0.25 4
rs7168592
CHSY1
15 101183294 intron variant C/T snv 9.8E-02 4
rs4924590
EHD4
15 41941475 intron variant T/A snv 0.30 3
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs10138752
RAD51B
14 68713254 intron variant C/T snv 8.8E-02 5
rs11624512
RIN3
14 92644775 non coding transcript exon variant C/T snv 0.15 5
rs11361923
NOXRED1
14 77396337 intron variant C/- delins 0.54 4
rs34061361
FLT3
13 28044450 intron variant AAA/-;A;AA;AAAA delins 5
rs1570884
RCBTB1
13 49547375 intron variant A/G snv 0.58 4
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs4761234 12 69338325 TF binding site variant T/C snv 0.36 5
rs555346412
HECTD4
12 112191863 intron variant G/C snv 8.2E-04 5
rs111930700
ACVR1B
12 51967869 intron variant C/G snv 8.4E-02 4
rs138488218 12 53354069 regulatory region variant A/T snv 7.6E-03 4
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs238914
ZBTB16
11 114113387 intron variant C/A snv 0.45 5
rs2846630
ZBTB16
11 114086475 intron variant G/A snv 0.35 5
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv 5