Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs7955371
WNK1
12 885321 missense variant G/C snv 1.00 0.99 1
rs7100433
ECHS1
10 133370298 intron variant T/C snv 0.98 3
rs2321168
STARD13 ; STARD13-AS
13 33279354 non coding transcript exon variant G/A snv 0.98 4
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs10919021
NOS1AP
1 162265600 intron variant C/T snv 0.97 1
rs2756231
SORCS1
10 106706654 intron variant C/T snv 0.98 0.97 1
rs453789
LOC105371789 ; HDAC5
17 44118647 intron variant A/C snv 0.97 1
rs567279
PDE4B
1 66222346 intron variant G/T snv 0.97 4
rs11784828
MSRA
8 10333788 intron variant T/G snv 0.97 1
rs6561821
STARD13
13 33287048 intron variant A/T snv 0.97 1
rs1337068
LOC105371475 ; NOS1AP
1 162163356 intron variant G/A snv 0.96 1
rs1572521
COL11A1
1 103097312 intron variant T/G snv 0.96 1
rs480392
NTNG1
1 107436774 synonymous variant A/C snv 0.99 0.95 3
rs2581473
MEF2A
15 99656452 intron variant A/G snv 0.95 1
rs4233488 1 41315341 intron variant T/C snv 0.94 1
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs6726798
VIL1
2 218436132 intron variant A/C snv 0.94 3
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93 5
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 1
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 1
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs2685289
RYR2
1 237746239 intron variant C/T snv 0.93 1
rs4402881
GLB1
3 33012839 intron variant T/C snv 0.93 2