Disease: Hormone measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs9472138
LOC107986598
0.882 0.160 6 43844025 downstream gene variant C/T snv 0.24 6
rs6885099
PDE8B
1.000 0.040 5 77234524 intron variant A/G snv 0.52 4
rs7860634
LHX3
9 136197833 intron variant G/A snv 0.55 4
rs10032216
LOC107986195
4 148748354 intron variant T/A;C snv 3
rs10799824
LOC105376819 ; LOC105376817 ; MICOS10
1 19514680 intron variant G/A snv 0.18 3
rs11624776 14 93129246 regulatory region variant A/C;T snv 3
rs11726248 4 170132368 intergenic variant G/A snv 6.8E-02 3
rs1537424
LINC00609
1.000 0.040 14 36104812 intron variant C/T snv 0.49 3
rs3813582
LINC01229 ; LOC105371356 ; MAFTRR
16 79715456 non coding transcript exon variant T/C snv 0.28 3
rs4804416
INSR
19 7223837 intron variant T/G snv 0.37 3
rs6499766
LPCAT2
16 55570216 intron variant A/T snv 0.54 3
rs7045138
PTCSC2
9 97829181 intron variant C/G;T snv 3
rs7240777 18 73500517 intergenic variant G/A snv 0.53 3
rs9497965
SASH1
1.000 0.040 6 148200156 regulatory region variant C/T snv 0.40 3
rs10519227
FAM227B ; FGF7
15 49454167 intron variant T/A snv 0.20 2
rs11755845
LINC01512
6 43937043 regulatory region variant C/T snv 0.21 2
rs13015993
LOC101928278
2 216760800 intron variant G/A snv 0.64 2
rs1571583
GLIS3
9 4267209 intron variant A/G snv 0.77 2
rs17723470
PRDM11
11 45206016 intron variant C/T snv 0.21 2
rs17776563 15 88575873 intergenic variant G/A;C snv 2
rs334699
NFIA
1 61154824 intron variant A/G snv 0.92 2
rs753760
PDE10A
6 165632995 intron variant C/A;G snv 2
rs7825175
NRG1
8 32558756 intron variant G/A snv 0.18 2