Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909658
FSHR
0.776 0.200 2 48983125 missense variant G/A snv 6.9E-04 5.8E-04 8
rs757975291
BRD2
0.851 0.120 6 32976868 missense variant G/A snv 4.1E-06 7.0E-06 4
rs386833511
FSHR
0.882 0.200 2 48963097 missense variant G/A snv 3
rs1440086679
BRD2
0.925 0.120 6 32979854 missense variant C/T snv 4.1E-06 2
rs121909661
FSHR
0.925 0.200 2 48963566 missense variant C/T snv 4.0E-06 2
rs1553387851
GTF2A1L ; STON1-GTF2A1L ; LHCGR
0.925 0.200 2 48698772 frameshift variant G/- delins 2
rs121908653
WNT4 ; LOC105376845
0.925 0.200 1 22142888 missense variant A/G snv 2
rs12190966
LOC100507557 ; FBXO30
1.000 0.040 6 145825684 intron variant T/G snv 0.46 1
rs1286391250
NANOS3
1.000 0.040 19 13877606 missense variant G/A snv 4.1E-06 1
rs954579305
RBMS3
1.000 0.040 3 29739726 missense variant G/A snv 1