Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs36217263
KL
1.000 0.040 13 33015697 upstream gene variant A/- del 0.21 4
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 4
rs1052700
PLIN1 ; KIF7
1.000 0.040 15 89665079 3 prime UTR variant A/T snv 0.26 3
rs12107
MYH9
1.000 0.040 22 36281936 3 prime UTR variant G/A;T snv 3
rs1228534100
HNF1A ; HNF1A-AS1
1.000 0.040 12 120978892 missense variant G/A snv 7.0E-06 3
rs192902098
PDX1
1.000 0.040 13 27920235 missense variant C/A;G;T snv 2.6E-03; 3.4E-04; 5.6E-05 3
rs2276047
INPPL1
1.000 0.040 11 72230337 intron variant A/G snv 0.28 0.33 3
rs3848403
FN3K
1.000 0.040 17 82736023 intron variant C/T snv 0.49 3
rs4253778
PPARA
1.000 0.040 22 46234737 intron variant G/C;T snv 3
rs7539020
AGT
1.000 0.040 1 230713444 intron variant C/T snv 0.43 3
rs7936247 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 3
rs867232360
GCK
1.000 0.040 7 44145552 missense variant C/T snv 3
rs1013773109
GRB14
1.000 0.040 2 164497436 missense variant T/C snv 2.1E-05 2
rs1036915
NTRK2
1.000 0.040 9 84822934 intron variant A/G snv 0.40 2
rs1042488900
ATF6
1.000 0.040 1 161802188 synonymous variant C/T snv 2
rs1042615
AVPR1A
1.000 0.040 12 63150429 missense variant A/C;G;T snv 0.60; 1.2E-05 2
rs10484821
LOC105378024
1.000 0.040 6 139547773 intron variant T/C snv 0.15 2
rs1060366
ATP1A1
1.000 0.040 1 116384040 synonymous variant A/G snv 1.3E-03 1.4E-03 2
rs10747983
AVPR1A
1.000 0.040 12 63144678 3 prime UTR variant G/A snv 0.29 2
rs10818684 1.000 0.040 9 122407651 intron variant C/T snv 0.62 2
rs11071657 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 2
rs11574
ID3
1.000 0.040 1 23559007 missense variant T/A;C snv 0.80 2
rs1169305
HNF1A
1.000 0.040 12 120999579 missense variant A/G snv 1.00 0.99 2
rs118081497
EEA1
1.000 0.040 12 92782070 missense variant A/T snv 1.1E-02 3.3E-03 2
rs1187274
NTRK2
1.000 0.040 9 84804874 intron variant C/G snv 0.55 2