Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 17
rs10436951
CEP170
1.000 0.080 1 243199378 intron variant A/G snv 7.1E-02 1
rs1045411
HMGB1
0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 2
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 11
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 9
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 4
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 2
rs1065852
NDUFA6-DT ; LOC112268294 ; CYP2D6
0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 2
rs10849605
RAD52
0.882 0.080 12 955272 intron variant T/C snv 0.49 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 15
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1
rs11008347
MALRD1
1.000 0.080 10 19072094 intron variant C/G snv 0.12 1
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 9
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 17
rs114002231 1.000 0.080 6 31459618 intron variant G/C snv 1
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 1
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 1
rs114385935
LOC105374996 ; LINC00533
1.000 0.080 6 28651576 upstream gene variant A/G snv 1