Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912532
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.776 0.280 2 48688065 missense variant C/A;G;T snv 1.2E-05 12
rs121912535
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.827 0.240 2 48688427 missense variant A/C snv 6
rs121912518
LHCGR ; STON1-GTF2A1L ; GTF2A1L
0.882 0.160 2 48688064 missense variant T/C;G snv 5
rs121912520
GTF2A1L ; STON1-GTF2A1L ; LHCGR
0.851 0.240 2 48688020 missense variant C/G snv 4
rs121912530
GTF2A1L ; STON1-GTF2A1L ; LHCGR
0.851 0.160 2 48687923 missense variant A/T snv 7.0E-06 4
rs121912525
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.882 0.240 2 48687950 missense variant G/T snv 2.0E-05 4.9E-05 3
rs760639637
CD44
0.925 0.160 11 35201784 missense variant A/G snv 4.0E-06 2
rs777212802
CD44
0.925 0.160 11 35201180 missense variant A/G snv 2
rs121912523
GTF2A1L ; LHCGR ; STON1-GTF2A1L
0.925 0.240 2 48688162 stop gained G/T snv 8.0E-06 2
rs121912529
GTF2A1L ; LHCGR ; STON1-GTF2A1L
0.925 0.160 2 48688737 missense variant C/T snv 2
rs140568136
GTF2A1L ; STON1-GTF2A1L ; LHCGR
1.000 0.160 2 48723638 stop gained C/A snv 8.0E-05 1.4E-05 2
rs1553387851
GTF2A1L ; STON1-GTF2A1L ; LHCGR
0.925 0.200 2 48698772 frameshift variant G/- delins 2
rs121912524
LHCGR ; STON1-GTF2A1L ; GTF2A1L
0.925 0.160 2 48688137 stop gained G/A snv 4.0E-06 1.4E-05 2
rs560462207
STON1-GTF2A1L ; GTF2A1L ; LHCGR
0.925 0.160 2 48688779 missense variant T/C snv 4.0E-06 2.8E-05 2
rs121912527
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.925 0.160 2 48723689 missense variant A/G snv 2
rs121912538
GTF2A1L ; LHCGR ; STON1-GTF2A1L
1.000 0.160 2 48688292 missense variant A/G snv 1
rs144859947
GTF2A1L ; LHCGR ; STON1-GTF2A1L
1.000 0.160 2 48687928 stop gained A/C;G;T snv 2.2E-04 1
rs121912536
LHCGR ; GTF2A1L ; STON1-GTF2A1L
1.000 0.160 2 48688770 missense variant A/T snv 1
rs121912539
LHCGR ; GTF2A1L ; STON1-GTF2A1L
1.000 0.160 2 48723650 missense variant C/A;G;T snv 1.2E-05; 4.0E-06; 2.8E-04 1
rs773279269
LHCGR ; STON1-GTF2A1L ; GTF2A1L
1.000 0.160 2 48725689 stop gained G/A;C snv 1
rs121912537
STON1-GTF2A1L ; GTF2A1L ; LHCGR
1.000 0.160 2 48688170 missense variant A/G snv 1