Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 8
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 7
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 7
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 6
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6