Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10028187
TMEM131L
4 153470288 intron variant A/G snv 0.31 1
rs10067881 5 95826771 upstream gene variant G/A snv 9.4E-02 1
rs10083830
SPECC1
17 20062570 intron variant G/A;C snv 1
rs10170266
INO80D
2 206080351 intron variant G/C snv 0.67 1
rs10206196
ADCY3
2 24914454 intron variant T/C snv 0.55 1
rs10211774
SMOX
20 4172971 intron variant G/A;C;T snv 1
rs10449752 1 56152275 intron variant T/A;G snv 1
rs1051904
SMOX
20 4182655 synonymous variant A/G snv 0.61 0.60 1
rs10587701
LINC00877
3 72238120 intron variant CT/- delins 1
rs10649609
COBLL1
2 164696196 non coding transcript exon variant -/AATAA;AGTAA delins 1
rs10710459 1 56467292 intron variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA;AAAAAAA;AAAAAAAA delins 0.87 1
rs10716631
PNKD
2 218273447 intron variant T/G snv 1
rs10716881
SNORD59B ; ATP5F1B
12 56644387 intron variant A/-;AA delins 0.42 1
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 4
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs10769966
DENND2B
11 8825494 intron variant C/A;T snv 1
rs10828725
PRTFDC1
10 24929314 intron variant G/T snv 0.26 2
rs10840133
DENND2B
11 8824822 intron variant G/A snv 0.44 1
rs10897473
FLRT1 ; MACROD1
11 64085244 intron variant C/G;T snv 1
rs10911457
RGL1
1 183873970 intron variant T/C snv 0.55 1
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13 2
rs10954464 7 134700205 intergenic variant T/A snv 0.34 1
rs10999573
PCBD1
10 70884621 intron variant A/G snv 0.32 1
rs11014296
PRTFDC1
10 24913109 intron variant C/T snv 0.26 1
rs11021221 11 95575690 intron variant T/A;G snv 4