Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs903361
ADORA1
0.882 0.160 1 203122146 intron variant G/A;C snv 4
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2228530
PPP1CB
1.000 2 28778825 missense variant A/C;G snv 1
rs4674344
CYP27A1
1.000 2 218805152 intron variant A/T snv 0.53 1
rs951599607
PPARG
0.925 0.040 3 12434028 missense variant G/A snv 4
rs72563732
ADIPOQ-AS1 ; ADIPOQ
0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04 3
rs7643645
NR1I2
0.882 0.080 3 119806650 intron variant A/G snv 0.31 3
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs2290602
PPARGC1A
0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs17107315
SPINK1
0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs2071303
LOC108783645 ; HFE
0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 6
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9