Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10005540 4 173660916 downstream gene variant C/G;T snv 1
rs1000972 20 6641070 regulatory region variant T/A;G snv 2
rs10041818 5 148691691 intergenic variant C/T snv 0.35 1
rs10067798
TENM2
5 167413686 intron variant T/A snv 0.44 1
rs10088136 8 85482363 downstream gene variant T/A snv 0.64 1
rs1008833
PIK3C2B
1 204457167 intron variant A/G snv 0.12 3
rs10089933 8 48478923 intergenic variant T/C snv 0.32 1
rs10128597
TRIM66
11 8673283 intron variant G/A snv 0.27 1
rs1013105
SHROOM3
4 76687512 intron variant G/A;T snv 1
rs10136987 14 93842954 intergenic variant G/A snv 0.89 1
rs10141786
VRTN
14 74350715 intron variant A/G snv 0.67 2
rs10151945
ATXN3
14 92059269 3 prime UTR variant C/T snv 0.45 1
rs10157038
CASZ1
1 10652408 non coding transcript exon variant C/A;T snv 1
rs10168801
DIRC3
2 217715827 intron variant G/A snv 0.66 1
rs10172309
CCNYL1
2 207743915 intron variant G/C snv 2.7E-02 1
rs10184849
PCBP1-AS1
2 70034525 intron variant T/A;C snv 1
rs10201883 2 177606679 intron variant T/C snv 0.82 1
rs10209172
MFSD6 ; NEMP2
2 190504195 intron variant G/A;C snv 1
rs10214145 5 27636685 intergenic variant T/A;G snv 1
rs10283100
ENPP2
8 119583783 missense variant A/G;T snv 0.96 3
rs1035101 2 59563217 intron variant C/T snv 0.60 1
rs10410606
LTBP4
19 40603069 intron variant A/C snv 0.52 1
rs1041733 21 34311960 intron variant T/A snv 0.49 1
rs10438355
SMAD3
15 67195211 downstream gene variant C/G snv 0.20 1
rs1046874
LOC105371692 ; MDM4
1 204557932 3 prime UTR variant C/T snv 1