Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13405728
STON1-GTF2A1L ; LHCGR
0.790 0.200 2 48751020 intron variant A/G snv 0.15 8
rs2059807
INSR
0.851 0.200 19 7166098 intron variant A/G;T snv 7
rs4385527
AOPEP
0.827 0.280 9 94886305 intron variant G/A snv 0.31 6
rs10818854
DENND1A
0.851 0.200 9 123684499 intron variant G/A snv 5.7E-02 6
rs13429458
THADA
0.827 0.200 2 43411699 intron variant A/C snv 0.14 6
rs12478601
THADA
0.851 0.200 2 43494369 intron variant C/T snv 0.61 5
rs771470596
EDNRA
0.882 0.200 4 147539919 missense variant G/A;C snv 1.6E-05 4
rs104893844
UBA6-AS1 ; GNRHR
0.882 0.160 4 67754068 missense variant C/T snv 3.6E-05 7.0E-06 4