Source: ALL
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
rs10068521
PRLR
5 35230278 5 prime UTR variant G/A;C snv 1
rs1007888
MIF-AS1
0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46 4
rs10229583 1.000 0.080 7 127606849 downstream gene variant G/A snv 0.23 2
rs10245353 7 25818994 intergenic variant C/A snv 0.16 4
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10278590
LRRC61 ; RARRES2
7 150338437 missense variant T/A;C;G snv 1
rs1034395178
LZTR1
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06 33
rs1036483919
GCK
0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 4
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs1042531
PCK1
20 57565924 3 prime UTR variant T/G snv 0.45 1
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1042842
MFN2
1 12011623 3 prime UTR variant A/G snv 0.71 1
rs1050800
LPIN1
2 11825688 3 prime UTR variant C/T snv 0.12 1
rs10511544
PTPRD
9 10319881 intron variant A/C snv 0.32 1
rs1051295
KCNB1 ; LOC105372649
0.925 0.080 20 49372368 3 prime UTR variant A/G snv 0.22 3
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs10756026
PTPRD
9 10337976 intron variant T/A snv 0.34 1
rs10762264
LOC101928994
10 69217077 intron variant G/A snv 0.58 1
rs10770125
INS-IGF2 ; IGF2 ; IGF2-AS
0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
rs10802502
NLRP3
1 247448993 3 prime UTR variant C/T snv 0.55 1
rs10804591 3 129615390 intergenic variant C/A snv 0.63 5
rs10809070
PTPRD
9 10341235 intron variant C/G snv 0.30 1
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7