Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs12483959
PNPLA3
1.000 22 43930116 intron variant G/A;C;T snv 4
rs903361
ADORA1
0.882 0.160 1 203122146 intron variant G/A;C snv 4
rs951599607
PPARG
0.925 0.040 3 12434028 missense variant G/A snv 4
rs2290602
PPARGC1A
0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs1977081
PNPLA3
1.000 22 43934248 intron variant T/C;G snv 2
rs1007863
SAMM50 ; PARVB
1.000 22 43999571 missense variant T/A;C snv 0.44 1
rs2072905
PNPLA3
1.000 22 43937599 intron variant C/G;T snv 1
rs2228530
PPP1CB
1.000 2 28778825 missense variant A/C;G snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs72563732
ADIPOQ-AS1 ; ADIPOQ
0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04 3
rs17107315
SPINK1
0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs11090617
PNPLA3
1.000 22 43930820 intron variant C/T snv 0.18 1
rs2076211
PNPLA3
1.000 22 43933198 intron variant C/A;T snv 0.18 3
rs4823173
PNPLA3
0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 8