Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1003887
INSL3
0.882 0.240 19 17816591 3 prime UTR variant C/T snv 0.69 3
rs10152450
FEM1B
1.000 0.120 15 68279141 intron variant T/G snv 0.34 1
rs10179648
THADA
1.000 0.120 2 43580926 intron variant C/T snv 0.70 1
rs10305420
GLP1R
0.925 0.160 6 39048860 missense variant C/T snv 0.31 0.27 2
rs1038822
THADA
1.000 0.120 2 43511034 intron variant T/A;C snv 1
rs10407022
AMH ; MIR4321
0.882 0.200 19 2249478 missense variant G/T snv 0.77 0.74 3
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1044386
FEM1A
1.000 0.120 19 4795277 3 prime UTR variant G/A snv 0.20 1
rs1045435
PMEL ; RAB5B ; CDK2
1.000 0.120 12 55972376 3 prime UTR variant G/C snv 0.15 1
rs10459247
HSD17B6
1.000 0.120 12 56777732 intron variant T/C snv 0.21 1
rs1047233
INSL3
0.925 0.200 19 17821381 synonymous variant T/A;C;G snv 0.30 0.37 2
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10495960
GTF2A1L ; STON1-GTF2A1L ; LHCGR
1.000 0.120 2 48732893 missense variant G/A snv 0.18 0.14 1
rs10500204
INSR
0.882 0.160 19 7182952 intron variant A/C snv 0.25 3
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10505648
LINC02055
1.000 0.120 8 136144207 intron variant A/G snv 0.43 1
rs10514258
VCAN-AS1 ; VCAN
1.000 0.120 5 83575938 intron variant A/G snv 0.13 1
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1056917
RUVBL2 ; LHB
1.000 0.120 19 49016209 synonymous variant A/G snv 0.61 0.65 1
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1062809
FST
1.000 0.120 5 53484261 missense variant C/A;G snv 1
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs10739076 1.000 0.120 9 5440589 upstream gene variant A/C;T snv 1
rs10760321 1.000 0.120 9 124101917 TF binding site variant A/G snv 0.30 1