Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10042590 5 88477501 intron variant G/A snv 5.8E-02 1
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs1009358
LINC02576 ; LOC107984063 ; LINC02245
1.000 0.080 2 65049318 intron variant T/C snv 0.40 2
rs10107066
DPYSL2
8 26542619 intron variant G/C snv 0.29 1
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs1030431 8 58399138 intergenic variant A/G;T snv 3
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 6
rs1044486
USP36
17 78796097 3 prime UTR variant G/A snv 0.41 1
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs1047964
BACE1 ; RNF214
11 117286177 3 prime UTR variant G/A;C;T snv 1
rs1048070
FREM1
9 14735055 3 prime UTR variant T/C snv 0.46 1
rs10500326
UBN1
16 4868325 intron variant G/T snv 0.21 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1063857
VWF
12 6044348 synonymous variant A/G snv 0.31 0.40 2
rs10740995
CACNB2
10 18156159 intron variant G/A;T snv 1
rs1074703
NCALD
8 101803258 intron variant C/A snv 0.63 1
rs10748798
PAX2
10 100794914 intron variant C/T snv 0.91 1
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs10769254
MYBPC3
11 47340914 intron variant G/C snv 0.27 4
rs10786156
PLCE1
10 94254865 intron variant C/G snv 0.44 0.47 2
rs10816914
PALM2AKAP2
9 109998608 intron variant G/A snv 0.40 1