Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
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
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 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
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 3
rs2624265
LINC02694
15 38856448 intron variant T/C snv 0.28 2
rs2652822
LACTB ; RPS27L
15 63130573 3 prime UTR variant T/C snv 0.41 2
rs503279
FUT2 ; LOC105447645
19 48705753 3 prime UTR variant T/C snv 0.48 2
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2
rs9332998
CYP4A11
1 46938514 intron variant T/C snv 0.16 2
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 1
rs9358356
CDKAL1
1.000 0.080 6 20667151 intron variant T/C snv 0.39 1
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 2
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3