Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757417 1.000 0.040 9 23347855 intron variant G/A;T snv 2
rs1076884 1.000 0.040 16 13653946 intergenic variant C/G;T snv 2
rs10769859
EIF3F
1.000 0.040 11 7979900 intron variant G/A;C;T snv 1
rs10774037
CACNA1C
0.882 0.040 12 2311360 intron variant G/A snv 0.77 3
rs10786736
CNNM2 ; NT5C2
1.000 0.040 10 103089359 3 prime UTR variant G/C snv 9.9E-02 1
rs10789369 1.000 0.040 1 73359226 downstream gene variant A/G;T snv 1
rs10791097
LINC02551
1.000 0.040 11 130848735 intron variant T/G snv 0.60 2
rs10791098
LINC02551
1.000 0.040 11 130848816 intron variant T/G snv 0.58 1
rs10791106 1.000 0.040 11 130976537 intergenic variant A/G snv 0.45 2
rs10791111 1.000 0.040 11 130986204 intergenic variant T/G snv 0.45 2
rs10791946
ENPP7P7
1.000 0.040 11 67820541 intron variant A/G snv 0.41 1
rs10803138
SDCCAG8
1.000 0.040 1 243391917 intron variant A/G snv 0.77 1
rs1080500 1.000 0.040 3 53141001 intergenic variant G/A snv 0.27 2
rs10812518
IFT74
1.000 0.040 9 27041678 intron variant C/T snv 0.30 1
rs10812882
LINGO2
1.000 0.040 9 28891819 upstream gene variant T/C snv 0.56 1
rs10828317
PIP4K2A
0.776 0.280 10 22550699 missense variant T/C snv 1
rs10829461 1.000 0.040 10 128646955 intergenic variant G/A snv 0.14 1
rs10831912
TEAD1
1.000 0.040 11 12834867 intron variant T/C snv 0.54 2
rs10838634
LRP4
1.000 0.040 11 46908403 intron variant A/G;T snv 1
rs10860964
C12orf42
1.000 0.040 12 103202677 intergenic variant T/C snv 0.28 1
rs10863593
MIR29B2CHG
1.000 0.040 1 207844729 intron variant T/C snv 0.29 1
rs10866912
MROH6
0.925 0.080 8 143573145 upstream gene variant A/C;T snv 1
rs10878577 1.000 0.040 12 67200061 intergenic variant A/C snv 0.64 1
rs10883765
ARL3
1.000 0.040 10 102696929 intron variant T/C snv 0.11 1
rs10883795
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102894820 intron variant T/C snv 0.30 1