Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6471
CYP21A2
0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 24
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs523349
SRD5A2
0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs6165
FSHR
0.724 0.160 2 48963902 missense variant C/G;T snv 4.0E-06; 0.55 14
rs778139192
KIF7 ; TICRR
0.776 0.360 15 89629561 stop gained G/A;T snv 4.1E-06; 7.3E-05 14
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs6688832
H6PD
0.752 0.440 1 9263851 missense variant G/A;C snv 0.28; 1.2E-04 10
rs727479
MIR4713HG ; CYP19A1 ; MIR4713
0.790 0.240 15 51242350 intron variant C/A;T snv 10
rs628031
SLC22A1
0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 8
rs73598374
ADA
0.790 0.280 20 44651586 missense variant C/A;G;T snv 7.1E-06; 6.2E-02 8
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs2059806
INSR
0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7
rs2059807
INSR
0.851 0.200 19 7166098 intron variant A/G;T snv 7
rs683369
SLC22A1
0.807 0.360 6 160130172 missense variant G/A;C;T snv 4.0E-06; 0.83; 4.0E-06 7
rs1805017
PLA2G7
0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 5
rs4889
KISS1
0.882 0.160 1 204190659 missense variant G/A;C snv 5.2E-06; 0.29 5
rs6256
PTH
0.827 0.160 11 13492506 stop gained G/A;T snv 4.0E-06; 0.16 5
rs779829591
F3
0.827 0.320 1 94532395 missense variant G/A snv 4.0E-06 5
rs141012637
SERPINB10 ; SERPINB2
0.851 0.320 18 63901881 stop gained C/A;T snv 7.0E-05 4
rs184752888
BRD2
0.882 0.120 6 32977847 missense variant G/A snv 4