Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86 12
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 10
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 9
rs2079742
BCAS3
0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 7
rs2238732
PRODH
22 18927834 intron variant C/G;T snv 7
rs12613336 2 210704675 regulatory region variant T/C snv 0.19 6
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6
rs17450273 12 102967601 intergenic variant C/A;T snv 4
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 4
rs13244654
SUMF2
7 56079263 intron variant T/C snv 0.48 4
rs878521 7 44216044 downstream gene variant G/A snv 0.33 3
rs62149891
CCT4
2 61877999 intron variant A/G snv 1.0E-01 3
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 3
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 3
rs10265221
PRKAG2
7 151717243 intron variant T/A;C snv 3
rs75444260
PRKAR1B
7 635944 intron variant A/G snv 8.5E-02 3
rs7793921
PSPH ; CCT6A
7 56053188 intron variant G/A snv 0.64 3
rs774211
RBMS2
12 56527155 intron variant T/C snv 0.12 3
rs1986734
SHROOM3
1.000 0.120 4 76499631 intron variant C/T snv 0.43 3
rs10172053 2 210779923 intergenic variant T/C;G snv 2
rs10466351 11 92964815 upstream gene variant C/T snv 0.48 2