Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs17712208
PROX1-AS1
1 213977102 intron variant T/A snv 2.1E-02 2
rs340878
PROX1-AS1 ; PROX1
1 213983706 intron variant G/C snv 0.63 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2068834
ZNF512
0.925 0.120 2 27616672 intron 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 7
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 6
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs13404446
TRIM54
0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs4665965
MPV17
0.925 0.120 2 27313513 intron variant T/A;C snv 4
rs780110
IFT172
0.925 0.120 2 27462521 intron variant G/A snv 0.56 4
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3
rs2305929
RBKS ; MRPL33 ; BABAM2-AS1 ; BABAM2
1.000 0.040 2 27891044 intron variant A/G snv 0.14 3
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 3
rs1124649
TMEM214
2 27037601 missense variant G/A snv 0.32 0.35 2
rs11891554
PPM1G
2 27390750 intron variant G/A;T snv 7.1E-02 2
rs1395
SLC5A6
0.882 0.200 2 27201768 missense variant G/A snv 0.62 0.55 2
rs2390732
CERS6
2 168749457 intron variant G/A snv 0.65 2
rs3736594
MRPL33
2 27772914 intron variant A/C snv 0.62 2
rs563694
ABCB11
2 168917561 intron variant C/A snv 0.75 2
rs853787
ABCB11
2 168945742 intron variant G/A;T snv 2
rs13427272
CTNNA2
2 80058810 intron variant G/A snv 5.4E-02 1
rs13431652
SPC25
0.925 0.080 2 168896905 intron variant T/C snv 0.24 1