Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6166
FSHR
0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 17
rs6165
FSHR
0.724 0.160 2 48963902 missense variant C/G;T snv 4.0E-06; 0.55 14
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