Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 4
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 4
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 3
rs4149310
ABCA1
9 104826853 intron variant A/T snv 0.34 3
rs1912826
KLKB1
4 186228386 intron variant G/A;C snv 2
rs2657880
SPRYD4
12 56469986 3 prime UTR variant G/C snv 0.15 2
rs4788815
LOC105371334
16 71600908 intergenic variant A/T snv 0.69 2
rs10500569
LOC107984814
16 72722202 intron variant G/A;C;T snv 1
rs10502575 18 31756628 downstream gene variant A/G snv 6.9E-02 1
rs12051548
TM4SF5
17 4779740 intron variant G/C snv 7.5E-02 1
rs12507628 4 72779634 regulatory region variant G/A snv 0.13 1
rs1537370
CDKN2B-AS1
1.000 9 22084311 intron variant C/T snv 0.55 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
rs1851024 4 71842104 intergenic variant G/A snv 0.93 1
rs1998013 1 55492357 intron variant C/T snv 4.4E-03 1
rs2168889 4 74357994 intergenic variant A/G snv 4.7E-02 1
rs2306786
MYO1E
15 59195731 intron variant C/G snv 8.0E-02 1
rs2390582
LOC105378851
1 90478350 intergenic variant A/G snv 0.15 1
rs3798722
ELOVL2
6 11040190 intron variant A/G snv 0.39 1
rs7092929
LOC105376360 ; LINC02669
10 3496602 splice region variant A/C;T snv 1
rs712964 22 19168604 upstream gene variant T/C snv 0.66 1
rs741013
PRICKLE2
3 64306961 intron variant A/T snv 6.0E-02 1