Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201851995
RSRC1
3 158119720 intron variant TTAT/- delins 1.4E-04 2
rs35175632
ABHD17C
15 80745392 intron variant TT/-;T;TTT;TTTT delins 1
rs5794844
NCAM1
11 113089378 intron variant TT/-;T;TTT delins 0.54 1
rs150155092
ADARB2
10 1727688 intron variant TA/-;TATA delins 7.0E-06 1
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs11105364
ATP2B1
12 89675499 intron variant T/G snv 0.15 4
rs569550
LSP1
0.925 0.080 11 1865838 intron variant T/G snv 0.35 4
rs7483477
LINC01150
11 1899025 intron variant T/G snv 0.25 4
rs10832417
KCNQ1OT1 ; KCNQ1
11 2631427 non coding transcript exon variant T/G snv 0.32 3
rs453301 8 9172877 intron variant T/G snv 0.54 3
rs6669371
CLCN6
1 11822085 intron variant T/G snv 0.14 3
rs7299436
LOC107984543
12 89719293 intron variant T/G snv 0.14 3
rs9810888
CACNA1D
3 53601568 intron variant T/G snv 0.51 3
rs35427 12 115118502 intergenic variant T/G snv 0.40 2
rs448671
PLEKHA7
11 16878556 intron variant T/G snv 0.24 2
rs4775769
LOC105370809 ; FBN1
15 48647691 intron variant T/G snv 0.93 2
rs72831343
CABCOCO1
10 61755923 intron variant T/G snv 9.3E-02 2
rs76376137 6 34205553 regulatory region variant T/G snv 3.9E-02 2
rs1043069
XPR1
1 180890232 3 prime UTR variant T/G snv 0.38 1
rs10760117
PSMD5
9 120824459 non coding transcript exon variant T/G snv 0.59 0.48 1
rs10817007
SVEP1
9 110392967 intron variant T/G snv 0.15 1
rs11000752
BMS1P4-AGAP5 ; BMS1P4
10 73710597 intron variant T/G snv 0.12 1
rs113744258 12 65979721 intergenic variant T/G snv 0.51 1