Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10734649
SBF2-AS1 ; LINC02709
1.000 0.040 11 9759344 intron variant C/A;G;T snv 1
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42 3
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs10755578
LPA
0.925 0.040 6 160548706 intron variant C/G snv 0.44 0.42 1
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 1
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 5
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs1077534
FGD5
1.000 0.040 3 14836067 intron variant A/G snv 0.12 1
rs10793514 1.000 0.040 10 44001523 intergenic variant T/C snv 0.58 1
rs10806235
LINC02542
1.000 0.040 6 81993618 intron variant C/T snv 0.31 1
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 3
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 3
rs10818576
DAB2IP
1.000 0.040 9 121650669 intron variant T/G snv 0.21 2
rs10840293
SWAP70
1.000 0.040 11 9729649 intron variant G/A;C snv 2
rs10841443
LINC02398
1.000 0.040 12 20067099 intron variant C/G snv 0.56 1
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 1
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs10861032
C12orf42
0.925 0.040 12 103518728 non coding transcript exon variant T/C snv 0.24 1
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 1
rs10909862
ACTRT2
1.000 0.040 1 3020251 upstream gene variant G/A;C;T snv 1
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 2
rs10947789
KCNK5
0.925 0.080 6 39207146 intron variant T/C snv 0.18 1
rs10951983 1.000 0.040 7 6406396 downstream gene variant A/G snv 0.15 1