Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11887534
rs11887534
ABCG5 ; ABCG8
29 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 0.700 1.000 4 2007 2019
dbSNP: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 2 2016 2018
dbSNP: rs11012737
rs11012737
MLLT10
1 10 21560840 intron variant G/A snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs11641445
rs11641445 		1 16 11545628 downstream gene variant C/T snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs1169288
rs1169288
HNF1A ; HNF1A-AS1
21 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs12004
rs12004
KDELR3
1 22 38481456 missense variant T/G snv 0.29 0.27 0.700 1.000 1 2018 2018
dbSNP: rs12633863
rs12633863
TM4SF4
1 3 149493725 intron variant G/A snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs12882491
rs12882491
TRAF3
3 0.925 0.160 14 102816936 intron variant C/T snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs12968116
rs12968116
ATP8B1 ; LOC100505549
2 18 57655270 missense variant C/T snv 8.2E-02 8.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs13280055
rs13280055 		1 8 11664844 intergenic variant G/A snv 8.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs17138478
rs17138478
HNF1B ; LOC105371754
1 17 37713312 intron variant C/A;T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs17240268
rs17240268
ANPEP
1 15 89804583 missense variant G/A snv 6.9E-02 9.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs174567
rs174567
FADS1 ; FADS2
4 1.000 0.080 11 61825533 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1800961
rs1800961
HNF4A
21 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs1935
rs1935
JMJD1C
1 10 63168063 missense variant C/A;G;T snv 4.0E-06; 0.44 0.700 1.000 1 2018 2018
dbSNP: rs2070959
rs2070959
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A9
16 0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 0.700 1.000 1 2018 2018
dbSNP: rs212100
rs212100
SULT2A1
1 19 47873738 intron variant T/C snv 0.89 0.700 1.000 1 2018 2018
dbSNP: rs2290846
rs2290846
LRBA
3 1.000 0.040 4 150277928 missense variant G/A snv 0.20 0.18 0.700 1.000 1 2018 2018
dbSNP: rs2291428
rs2291428
MARCHF8 ; LOC105378286
1 10 45463408 missense variant G/C snv 0.24 0.23 0.700 1.000 1 2018 2018
dbSNP: rs2292553
rs2292553
PNKD ; TMBIM1 ; MIR6513
2 2 218282080 missense variant G/A snv 0.55 0.43 0.700 1.000 1 2018 2018
dbSNP: rs2469991
rs2469991 		1 8 119335236 intergenic variant A/T snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs2547231
rs2547231
SULT2A1
2 19 47881800 intron variant C/A snv 0.86 0.700 1.000 1 2016 2016
dbSNP: rs28929474
rs28929474
SERPINA1
37 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs34851490
rs34851490 		1 19 45881296 downstream gene variant A/G snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs4148808
rs4148808
ABCB4
1 7 87476479 intron variant T/C snv 0.19 0.700 1.000 1 2018 2018