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: rs10513686
rs10513686
SLC2A2
1 3 171007753 intron variant G/A snv 0.21 0.800 1.000 1 2011 2011
dbSNP: rs1076540
rs1076540
MICAL3
1 22 17957192 intron variant C/T snv 0.21 0.800 1.000 1 2011 2011
dbSNP: rs10908458
rs10908458 		1 1 155154472 intergenic variant T/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs1169288
rs1169288
HNF1A ; HNF1A-AS1
21 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 0.800 1.000 1 2012 2012
dbSNP: rs12145922
rs12145922
PKN2-AS1
2 1 88680551 intron variant C/A snv 0.57 0.800 1.000 1 2011 2011
dbSNP: rs12968116
rs12968116
ATP8B1 ; LOC100505549
2 18 57655270 missense variant C/T snv 8.2E-02 8.0E-02 0.800 1.000 1 2011 2011
dbSNP: rs13030978
rs13030978
MYO1B
1 2 191252512 intron variant C/T snv 0.24 0.800 1.000 1 2011 2011
dbSNP: rs1335645
rs1335645
CEPT1 ; DRAM2
1 1 111141654 intron variant A/G;T snv 0.15 0.800 1.000 1 2011 2011
dbSNP: rs17145750
rs17145750
MLXIPL
9 0.925 0.120 7 73612048 intron variant C/A;T snv 0.800 1.000 1 2011 2011
dbSNP: rs2073398
rs2073398
GGT1
1 22 24603137 intron variant C/G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs2140773
rs2140773
EFHD1
1 2 232648465 intron variant C/A;G snv 0.61 0.800 1.000 1 2011 2011
dbSNP: rs2739330
rs2739330 		1 22 23953099 intron variant T/C snv 0.58 0.800 1.000 1 2011 2011
dbSNP: rs4503880
rs4503880 		1 18 58416822 non coding transcript exon variant T/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs4547811
rs4547811
ZNF827
1 4 145873469 intron variant T/C snv 0.20 0.800 1.000 1 2011 2011
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
10 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.800 1.000 1 2011 2011
dbSNP: rs6888304
rs6888304 		1 5 31020414 intergenic variant A/G snv 0.30 0.800 1.000 1 2011 2011
dbSNP: rs7310409
rs7310409
HNF1A
7 0.925 0.160 12 120987058 intron variant A/C;G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs754466
rs754466
DLG5
1 10 77920676 intron variant A/G;T snv 0.22 0.800 1.000 1 2011 2011
dbSNP: rs8038465
rs8038465
CD276
1 15 73685996 intron variant C/T snv 0.31 0.800 1.000 1 2011 2011
dbSNP: rs9296736
rs9296736
MLIP
1 6 54059899 intron variant T/C snv 0.51 0.800 1.000 1 2011 2011
dbSNP: rs9913711
rs9913711
SOX9-AS1 ; LINC02097
1 17 72102020 intron variant G/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs10458877
rs10458877
LINC02682
1 11 15919553 intron variant C/T snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs10460702
rs10460702
LOC105372767
1 21 29182833 intron variant G/A snv 2.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs10497655
rs10497655
ZNF804A ; LOC105373780
2 1.000 0.040 2 184597314 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10913568
rs10913568
TEX35 ; C1orf220
1 1 178544276 intron variant C/T snv 0.40 0.700 1.000 1 2018 2018