Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72840032
CYP2C23P
10 100130207 intron variant C/T snv 3.4E-02 1
rs149578709
ADAMTS17
15 100132203 intron variant A/G snv 9.0E-03 5.2E-03 1
rs10148930
EVL
14 100134466 intron variant A/G;T snv 1
rs11677607
AFF3
2 100134688 intron variant C/T snv 0.24 1
rs73966422
AFF3
2 100137627 non coding transcript exon variant C/G;T snv 1
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs11692867
AFF3
2 100143015 intron variant G/A snv 0.34 1
rs11123811
AFF3
1.000 0.120 2 100143710 intron variant T/C snv 0.55 1
rs2309752
AFF3
2 100145707 intron variant T/A;G snv 1
rs368755101
AFF3
2 100145754 intron variant G/- del 9.7E-04 1
rs4851253
AFF3
2 100146324 intron variant T/G snv 0.44 1
rs4851254
AFF3
2 100146475 intron variant C/G;T snv 1
rs13415465
AFF3
2 100147542 intron variant T/G snv 0.37 1
rs13415583
AFF3
1.000 0.120 2 100147625 intron variant T/G snv 0.37 1
rs10496344
AFF3
2 100147663 intron variant T/C;G snv 1
rs17789218
LOC105377911
6 100152221 intergenic variant T/A;C snv 3
rs1408579
ERLIN1
1.000 0.040 10 100152437 intron variant C/T snv 0.32 3
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs9496567
LOC105377911
6 100154877 intergenic variant G/A snv 0.24 2
rs400301
CIDECP1
3 10015782 intron variant G/A snv 6.8E-02 1
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 1
rs2503099
LOC105377911
6 100162225 regulatory region variant A/G snv 0.18 1
rs6857001
LOC105374476 ; SLC2A9
4 10016456 intron variant G/A snv 0.32 1
rs2184971
PCCA
1.000 13 100165838 intron variant A/G snv 0.49 1
rs11123816
AFF3
2 100167191 intron variant G/A snv 0.20 1