Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs7860634
LHX3
9 136197833 intron variant G/A snv 0.55 4
rs951366
NUCKS1
0.925 0.240 1 205716224 3 prime UTR variant T/C snv 0.34 4
rs9356988
SLC17A1 ; SLC17A4
0.925 0.120 6 25777253 3 prime UTR variant G/A snv 0.28 4
rs11726248 4 170132368 intergenic variant G/A snv 6.8E-02 3
rs7240777 18 73500517 intergenic variant G/A snv 0.53 3
rs4954192
CCNT2-AS1 ; ACMSD
1.000 0.080 2 134875411 intron variant C/T snv 0.52 3
rs6499766
LPCAT2
16 55570216 intron variant A/T snv 0.54 3
rs7045138
PTCSC2
9 97829181 intron variant C/G;T snv 3
rs17185536 1.000 0.080 6 100173055 upstream gene variant C/G;T snv 2
rs749618 19 52112198 upstream gene variant A/G snv 0.13 2
rs76465767 12 122901948 TF binding site variant T/C snv 2.4E-02 2
rs67142165
EPHB2
1 22884066 intron variant C/T snv 8.2E-02 2
rs7020640
HSPC324 ; LOC102724193 ; EGFL7
9 136653172 intron variant C/T snv 0.21 2
rs12534332
LOC105375586
7 155214802 intron variant G/A snv 0.59 2
rs58926603
LOC107985017
17 6438550 upstream gene variant A/G snv 0.47 2
rs2066773
MAPK12
22 50257071 non coding transcript exon variant G/A;C snv 2.0E-02; 4.0E-06 2
rs10818937 9 124253161 upstream gene variant C/T snv 0.24 1
rs10946313 6 19381155 intron variant T/C snv 0.41 1
rs118024684 8 46506475 intergenic variant T/A snv 2.9E-02 1
rs56069042 18 60247411 intergenic variant A/G snv 2.4E-02 1
rs7694879 4 170048648 regulatory region variant C/T snv 6.1E-02 1
rs7951105 11 39010243 intergenic variant T/A;G snv 0.79 1