Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12129573
LOC105378800
0.925 0.040 1 73302683 upstream gene variant C/A snv 0.31 2
rs12139351 1.000 0.040 1 199471855 intergenic variant G/A snv 0.21 2
rs12407717 0.925 0.040 1 29953167 intergenic variant C/T snv 0.11 2
rs12410444
LOC101929592 ; ST3GAL3
1.000 0.040 1 43723048 intron variant A/G snv 0.25 2
rs1490191 1.000 0.040 1 151944275 upstream gene variant C/A snv 0.90 2
rs1498232 1.000 0.040 1 29961104 regulatory region variant T/C snv 0.53 2
rs17659437 1.000 0.040 1 177337251 intergenic variant T/C snv 0.13 2
rs1782810
MIR137HG
1.000 0.040 1 98036784 intron variant G/A;T snv 2
rs2015244 1.000 0.040 1 29956096 intergenic variant A/T snv 0.54 2
rs2143103 1.000 0.040 1 22103576 downstream gene variant G/A;T snv 2
rs2256126
SDCCAG8
1.000 0.040 1 243340806 intron variant A/G snv 0.27 2
rs2297797
CYB561D1
1.000 0.040 1 109498058 3 prime UTR variant C/T snv 0.37 2
rs2318763
VPS45
0.925 0.040 1 150143798 intron variant A/G snv 0.15 2
rs236318
BCAR3
1.000 0.040 1 93584664 intron variant C/G snv 0.79 2
rs2477432
RAP1A
1.000 0.040 1 111642655 intron variant T/A snv 0.52 2
rs3001723
PTPRF
0.925 0.040 1 43572014 intron variant G/A snv 0.40 2
rs301798
RERE ; RERE-AS1
1.000 0.040 1 8428505 non coding transcript exon variant A/G snv 0.30 2
rs302719
RERE-AS1 ; RERE
1.000 0.040 1 8430260 intron variant T/G snv 0.33 2
rs35771425 1.000 0.040 1 211436426 downstream gene variant T/C;G snv 2
rs35998080
LINC02797
1.000 0.040 1 72812932 intron variant G/T snv 0.37 2
rs4654748
NBPF3
1.000 0.040 1 21459575 intron variant C/T snv 0.38 2
rs4657175
NOS1AP
1.000 0.040 1 162225948 intron variant T/C;G snv 2
rs482039 1.000 0.040 1 190808437 intergenic variant C/T snv 9.1E-02 2
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 2
rs589249
LOC105378648 ; LOC107984941
1.000 0.040 1 36696751 intergenic variant A/G;T snv 2