Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886041065
ASXL2
0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 38
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 14
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 9
rs1057515572
PMS2
0.882 0.200 7 5987033 frameshift variant GC/ACT delins 8
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 7
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 7
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 7
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 6
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 5
rs587777732
MIR3646 ; HNF4A
0.763 0.240 20 44406195 missense variant C/T snv 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 4
rs1057518775
KCNJ11
0.851 0.160 11 17387907 missense variant G/A;C snv 4
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 4
rs2014355
ACADS
0.925 0.120 12 120737721 non coding transcript exon variant T/C snv 0.22 3
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 3
rs193922479
HNF4A
0.925 0.080 20 44424116 missense variant C/A;T snv 8.0E-06 7.0E-06 2
rs683369
SLC22A1
0.807 0.360 6 160130172 missense variant G/A;C;T snv 4.0E-06; 0.83; 4.0E-06 2
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 1
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 1
rs121909730
GLUD1
0.882 0.040 10 87053380 missense variant G/A snv 1
rs121909731
GLUD1
0.851 0.120 10 87057692 missense variant G/A;C snv 4.0E-06 1