Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 36
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 26
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 22
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 21
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 19
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 18
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 17
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 15
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13