Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 10
rs2544390
LRP2
0.925 0.080 2 169348336 intron variant C/T snv 0.45 4
rs10786691
SUFU
0.925 0.160 10 102604895 intron variant G/A;T snv 3
rs2071045
LEP
0.925 0.120 7 128252927 intron variant T/C snv 0.18 3
rs34396413
TFAP2A
0.925 0.160 6 10400802 intron variant AGA/- delins 6.8E-02 6.9E-02 3
rs3832406
MTHFD1L
0.925 6 150898848 intron variant -/A;ATA;ATTATG ins 5.8E-05; 4.3E-05 2.1E-05 3
rs12132032
PRKACB
1.000 0.080 1 84100906 intron variant A/G snv 0.41 2
rs2797840
SARDH
1.000 0.080 9 133671511 intron variant G/A;C snv 0.53; 1.1E-04 2
rs3814573
TCF7L2
1.000 0.080 10 113138334 intron variant T/C snv 0.71 2
rs452159
ADA
1.000 0.040 20 44642461 intron variant G/T snv 0.28 2
rs502396
TYMS ; TYMSOS
1.000 0.080 18 659236 intron variant C/T snv 0.46 2
rs10827337
PARD3
10 34202922 intron variant G/A snv 0.20 1
rs10925260
MTR
1 236884786 intron variant A/C snv 0.56 1
rs11247593
ARID1A
1 26725589 intron variant G/A snv 0.30 1
rs12218196
PARD3
10 34196864 intron variant T/C snv 2.0E-02 1
rs1256146
MTHFD1 ; ZBTB25
14 64453947 intron variant G/A snv 0.17 1
rs17187449
KCNB2
8 72830736 intron variant G/A snv 1
rs1956545 14 64386187 intron variant C/T snv 0.92 1