Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 1
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 1
rs1406948
UQCC1
20 35317816 intron variant G/A snv 0.44 1
rs2076529
TSBP1-AS1 ; BTNL2
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 2
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs6701231
TBX15
1 118953038 intron variant C/A;G snv 1
rs984222
TBX15
1 118961220 intron variant C/A;G snv 1
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs7745274
RSPO3 ; LOC112267972
6 127188012 intron variant G/A snv 0.56 1
rs9491696
RSPO3
6 127131494 intron variant C/G snv 0.45 1
rs6931262
RREB1
6 7217284 non coding transcript exon variant C/T snv 0.10 1
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 2
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 1
rs620861
PCAT1 ; CASC8 ; POU5F1B ; CASC21
0.925 0.080 8 127323428 intron variant G/A snv 0.36 1
rs10894604
OPCML
11 132771851 non coding transcript exon variant T/G snv 0.26 1
rs3088050
NSD1
5 177299634 3 prime UTR variant G/A snv 0.18 1
rs17109256
NRXN3
14 79473650 intron variant G/A snv 0.21 1
rs6486060
NRIP3 ; LOC105376541
11 9003083 intron variant G/A snv 0.55 1
rs6784615
NISCH
1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 1