Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2292989
COL16A1 ; LOC101929444
1 31670172 non coding transcript exon variant A/G snv 0.33 2
rs3738814
ATP13A2
1 17005181 intron variant A/G snv 0.52 2
rs3814333
COLGALT2
1 184037985 upstream gene variant C/T snv 0.29 2
rs55745410
PHC2
1 33337216 intron variant A/G snv 0.28 2
rs6422513
EVI5
1 92566910 intron variant G/A;C snv 2
rs6587515 1 150636412 regulatory region variant G/A snv 7.2E-02 2
rs66461782
ZRANB2-AS1 ; ZRANB2 ; MIR186
1 71067604 intron variant A/T snv 0.32 0.27 2
rs6684205
TGFB2
1 218436360 intron variant A/G;T snv 2
rs7534091 1 118321993 intergenic variant A/G snv 0.23 2
rs78444298
EDEM3
1 184702964 missense variant G/A snv 1.2E-02 1.2E-02 2
rs823118 0.925 0.080 1 205754444 upstream gene variant C/A;T snv 2
rs945631
DIPK1A
1 92960610 intron variant G/A snv 4.1E-02 2
rs991967
TGFB2-OT1 ; TGFB2
1 218442109 3 prime UTR variant A/C snv 0.37 2
rs1006224
C1orf21
1 184572468 intron variant G/A snv 0.40 1
rs10157941
PODN
1 53083314 intron variant C/G snv 0.25 1
rs10218741
LOC101929750
1 221106893 regulatory region variant G/A;C snv 1
rs10305677
ARNT
1 150846616 intron variant T/A snv 1.8E-02 1
rs1044145
YOD1 ; PFKFB2
1 207044014 3 prime UTR variant T/A;C snv 1
rs10737515
MGST3
1 165630223 upstream gene variant G/A;C snv 1
rs10779364
ZC3H11B
1 219614071 upstream gene variant G/C snv 0.56 1
rs10793765
LOC105371692
1 204580247 intergenic variant A/G;T snv 1
rs10797816
LAMC1
1 183029351 intron variant A/T snv 0.54 1
rs10798580 1 177895419 intron variant G/A snv 0.36 1
rs10799445 1 227724182 upstream gene variant A/C snv 0.27 1
rs10857961
ST7L
1 112539531 intron variant C/A;T snv 1