Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 3
rs10511701
CDKN2B-AS1
9 22112600 intron variant T/A;C snv 2
rs1333043
CDKN2B-AS1
9 22106732 intron variant T/A snv 0.64 2
rs1912826
KLKB1
4 186228386 intron variant G/A;C snv 2
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 2
rs2657880
SPRYD4
12 56469986 3 prime UTR variant G/C snv 0.15 2
rs7341786
CDKN2B-AS1
9 22112242 intron variant A/C snv 0.65 2
rs7859362
CDKN2B-AS1
9 22105928 intron variant T/C snv 0.64 2
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 1
rs10502575 18 31756628 downstream gene variant A/G snv 6.9E-02 1
rs10807323
PHACTR1
6 12794799 intron variant G/A snv 0.34 1
rs1333050
CDKN2B-AS1
9 22125914 intron variant C/T snv 0.50 1
rs1537371
CDKN2B-AS1
9 22099569 intron variant C/A;T snv 1
rs1556516
CDKN2B-AS1
9 22100177 intron variant G/A;C snv 1
rs16850360 4 74006728 intron variant A/G snv 4.2E-02 1
rs16939881
ALDH1A2 ; AQP9
15 58179780 intron variant G/C;T snv 1
rs17404667
PRICKLE2
3 64288876 intron variant C/G snv 6.2E-02 1
rs188234402
CDKN2B-AS1
9 22029058 intron variant T/A snv 2.1E-05 1
rs201049435
CDKN2B-AS1
9 22029059 intron variant AA/-;A;AAA;AAAA delins 6.9E-03 1
rs2390582
LOC105378851
1 90478350 intergenic variant A/G snv 0.15 1
rs34059530
CDKN2B-AS1
9 22029059 intron variant AA/-;A;AAA;AAAA delins 1
rs3798722
ELOVL2
6 11040190 intron variant A/G snv 0.39 1
rs397733626
CDKN2B-AS1
9 22029059 intron variant AA/-;A;AAA;AAAA delins 0.58 1
rs4451405
CDKN2B-AS1
9 22071751 intron variant C/T snv 0.69 1
rs4711863
PHACTR1
6 12915185 intron variant G/C snv 0.29 1