Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003688
SCGN
6 25658944 intron variant G/A snv 0.14 2
rs1008084
CCDC162P
6 109305762 intron variant G/A snv 0.40 2
rs1010222
CALR
19 12937794 upstream gene variant A/G snv 0.70 3
rs10159477
HK1
10 69340132 intron variant G/A snv 0.14 2
rs10168349
PRKCE
2 46133768 intron variant G/C snv 0.36 2
rs10184620
PRKCE
2 46131396 intron variant A/G snv 0.12 2
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 2
rs1022506
MYB
6 135190449 intron variant G/A snv 0.10 2
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10404876
DNASE2
19 12876791 intron variant T/A;C snv 2
rs1041479 6 135167358 regulatory region variant T/A;C snv 2
rs10419408
HOOK2 ; LOC105372281 ; RTBDN
19 12831936 intron variant A/G snv 0.33 2
rs10426080
MAST1 ; HOOK2
19 12847036 intron variant A/G snv 0.40 2
rs10434845
CARMIL1
6 25582529 intron variant C/G snv 0.38 2
rs10445937 2 60410521 intron variant G/A snv 0.39 3
rs10457631 6 135124041 intergenic variant A/C snv 0.25 2
rs10457632 6 135124064 intergenic variant A/G snv 0.33 2
rs1046276
CTF1
1.000 0.040 16 30903305 3 prime UTR variant T/C snv 0.62 1
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 4
rs10484494
LOC105378010
6 135108955 regulatory region variant G/A snv 4.8E-02 2
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 3
rs10498725
CARMIL1
1.000 0.040 6 25454787 intron variant C/T snv 0.17 3
rs10498752
USP49
6 41800772 intron variant T/C snv 0.53 2
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 1
rs1051130
CCND3
6 41936044 missense variant A/C;G;T snv 0.54; 1.6E-05 1