Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10068737 5 118700852 intergenic variant T/A;C snv 1
rs1009840
SGK1 ; LOC107986646
6 134225547 intron variant G/A snv 0.53 1
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 1
rs102274
TMEM258
1.000 0.080 11 61790354 non coding transcript exon variant T/C snv 0.28 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs10774021
SLC6A13
1.000 0.080 12 240132 intron variant C/T snv 0.57 1
rs1077989
GPHN ; TMEM229B
1.000 0.080 14 67509105 intron variant A/C snv 0.39 1
rs10794720
WDR37
1.000 0.080 10 1110225 intron variant T/C snv 0.89 1
rs11078903
CDK12
17 39475671 intron variant G/A;C;T snv 2
rs1168357
GRIP1
12 66356099 intron variant T/C snv 0.50 1
rs1171614
SLC16A9
0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 2
rs1171616
SLC16A9
0.882 0.200 10 59708831 intron variant G/T snv 0.79 2
rs11959928
DAB2 ; C9
1.000 0.080 5 39397030 intron variant T/A snv 0.39 1
rs12124078
DNAJC16
1 15543404 intron variant A/G snv 0.32 1
rs12373237
LAMA3
0.851 0.200 18 23845972 intron variant G/A snv 0.47 1
rs12460876
SLC7A9
1.000 0.080 19 32865985 intron variant T/C snv 0.36 1
rs12575381 11 135033566 regulatory region variant G/A snv 0.16 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 2
rs12922822
UMOD
1.000 0.040 16 20356323 upstream gene variant C/A;T snv 1
rs13538
NAT8 ; ALMS1P1
1.000 0.080 2 73641201 missense variant A/G snv 0.21 0.31 3
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 3
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 3
rs1500896
C8orf37-AS1
8 95474454 intron variant G/A;C snv 1