Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10139403
DLK1
1.000 0.040 14 100728224 intron variant A/G snv 0.62 1
rs1018185646
HNF4A
1.000 0.040 20 44428455 missense variant T/C snv 4.0E-06 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894006
GCK ; LOC105375258
0.925 0.040 7 44149992 stop gained G/A;T snv 1.2E-05 1
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 7
rs10515074
PIK3R1
0.925 0.120 5 68270365 intron variant A/G;T snv 2
rs1064793998
GCK
0.882 0.080 7 44153325 missense variant C/T snv 2
rs10770125
INS-IGF2 ; IGF2 ; IGF2-AS
0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
rs11202592
KLLN ; PTEN
0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03 5
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 15
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 10
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 21
rs1272388614
ABCC8
0.851 0.080 11 17395658 missense variant C/T snv 2.4E-05 3.5E-05 5
rs12836771
HTR2C ; MIR1912 ; MIR1264
0.882 0.080 X 114650913 intron variant A/G snv 0.12 4
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 17
rs13412852
LPIN1
0.851 0.120 2 11774815 intron variant C/T snv 0.26 4
rs137853238
HNF1A
0.807 0.200 12 120994265 missense variant G/A snv 3
rs137853240
HNF1A
0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 7
rs1410713 1.000 0.040 20 3079704 downstream gene variant A/C snv 0.62 1