Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs275645 3 148746667 downstream gene variant G/A snv 0.43 1
rs909221872
ACOT7
1 6349856 missense variant G/T snv 1
rs1800038
ADRA2A
10 111079134 synonymous variant C/A snv 7.4E-02 4.9E-02 1
rs201607471
ADRB3
8 37966397 missense variant C/T snv 8.5E-06 1
rs2328549
CDKAL1
6 20718009 intron variant A/T snv 0.18 1
rs6938256
CDKAL1
6 20887723 intron variant G/A;T snv 1
rs7598922
DHX57
2 38855202 missense variant T/C snv 0.62 0.54 1
rs587780343
GCK
7 44145638 missense variant C/A;T snv 1
rs587780347
GCK ; LOC105375258
7 44147807 missense variant C/T snv 1
rs2394529
HKDC1 ; LOC101928994
10 69225511 intron variant G/A;C snv 1
rs2254514
IL15
4 141719385 5 prime UTR variant T/A;C snv 1
rs2585
INS-IGF2 ; IGF2
11 2129214 3 prime UTR variant T/C;G snv 1
rs231841
KCNQ1
11 2702374 intron variant G/T snv 0.45 1
rs7929804
KCNQ1OT1 ; KCNQ1
11 2619594 non coding transcript exon variant G/A snv 0.49 1
rs4820294
LGALS1
22 37675036 upstream gene variant G/A snv 0.30 1
rs10762264
LOC101928994
10 69217077 intron variant G/A snv 0.58 1
rs9645501
LOC101928994 ; HKDC1
10 69227010 intron variant G/A snv 0.43 1
rs1050800
LPIN1
2 11825688 3 prime UTR variant C/T snv 0.12 1
rs10278590
LRRC61 ; RARRES2
7 150338437 missense variant T/A;C;G snv 1
rs1042842
MFN2
1 12011623 3 prime UTR variant A/G snv 0.71 1
rs10802502
NLRP3
1 247448993 3 prime UTR variant C/T snv 0.55 1
rs712699
PAX4
7 127610543 3 prime UTR variant G/A snv 0.75 1
rs1042531
PCK1
20 57565924 3 prime UTR variant T/G snv 0.45 1
rs2236745
PCK1
20 57561937 non coding transcript exon variant T/C snv 0.44 1
rs10068521
PRLR
5 35230278 5 prime UTR variant G/A;C snv 1