Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6711493
DARS1
2 135934983 intron variant A/G snv 0.23 2
rs7180079
CSNK1G1
15 64337674 intron variant A/G snv 0.79 2
rs730775
NFKBIE
1.000 0.080 6 44264337 intron variant A/G snv 0.36 2
rs73217470 13 71939282 intergenic variant A/G snv 3.4E-02 2
rs7516138
PIK3CD
1 9651584 upstream gene variant A/G snv 0.52 2
rs78697948
IKZF1
7 50369033 3 prime UTR variant A/G snv 5.7E-02 2
rs9480737 6 107121073 intergenic variant A/G snv 0.33 2
rs9551434
FLT3
13 28067434 intron variant A/G snv 0.18 2
rs9554228
FLT3
13 28063701 intron variant A/G snv 0.60 2
rs45577137
CEBPD
8 47739071 upstream gene variant A/G;T snv 4
rs10980797
LOC105376219
9 111150273 intron variant A/G;T snv 3
rs10147992
STXBP6
14 25034593 intron variant A/G;T snv 2
rs4919087 10 97312750 upstream gene variant A/G;T snv 2
rs514406
ZYG11A
1 52864786 intron variant A/G;T snv 2
rs62569723
LOC105376219
9 111174639 intron variant A/G;T snv 2
rs28722705
ANKRD55
5 56158115 intron variant A/T snv 9.9E-02 3
rs2507971
MICB-DT ; MICB
6 31493595 intron variant A/T snv 0.59 2
rs562398803 20 50492033 regulatory region variant AA/-;A;AAA;AAAA;AAAAA delins 2
rs66645127
RCBTB1
13 49549135 intron variant AAA/-;A;AA;AAAA;AAAAAA delins 0.64 2
rs71355435 17 40013327 intron variant AAAAAAA/-;A;AA;AAA;AAAA;AAAAA;AAAAAA;AAAAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAA;AAAAAAAAAAAAAAA delins 0.30 2
rs67397717
CRYBG2
1 26327482 intron variant AAAAAAA/-;AAAA;AAAAA;AAAAAA;AAAAAAAA delins 2
rs148550456
LOC105374570 ; LINC02580
2 43124884 intron variant ACAC/-;AC;ACACAC;ACACACAC delins 2
rs34834119
ETS1
11 128463122 intron variant AT/- del 0.26 2
rs146723115 8 67901594 intergenic variant AT/-;ATAT;ATATAT;ATATTTATATATAATATATATAATTTATATATATATATATAT delins 2
rs11327184
CCDC26
8 129592027 intron variant C/- delins 0.40 4