Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs6471
CYP21A2
0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 24
rs2281939
SORBS1
0.790 0.320 10 95414595 missense variant T/C snv 8.2E-02 0.13 9
rs9378251
CYP21A2
0.776 0.320 6 32038514 missense variant C/T snv 9.2E-05 5.4E-04 8
rs768768839
POMC
0.807 0.280 2 25161679 missense variant G/A snv 5.6E-06 6
rs8111699
STK11
0.851 0.200 19 1209715 intron variant C/G snv 0.53 6
rs757033996
HSD3B2
0.882 0.200 1 119419519 missense variant G/A snv 2.0E-05 4.9E-05 3
rs772953044
ACOT7
0.925 0.120 1 6333503 missense variant T/C;G snv 4.0E-06; 4.0E-06 2
rs1324026337
TGM2
0.925 0.120 20 38148038 missense variant T/C snv 4.0E-06 2
rs752163489
TMPRSS6
0.925 0.120 22 37096044 stop gained C/A;T snv 1.8E-04 2