Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10006235
LINC02466
1.000 0.040 4 129748953 non coding transcript exon variant T/C snv 0.73 2
rs10012947 1.000 0.040 4 30491805 regulatory region variant C/T snv 0.33 1
rs1001684 1.000 0.040 5 40810324 intergenic variant C/A snv 0.29 1
rs1002424
PRKAA1
1.000 0.040 5 40767295 intron variant A/G snv 0.31 1
rs10046758
CSMD1
1.000 0.040 8 4326648 non coding transcript exon variant C/G;T snv 1
rs10061788
LINC00461
1.000 0.040 5 88638889 intron variant G/A;T snv 2
rs10065570
RPL37
1.000 0.040 5 40835525 upstream gene variant C/T snv 0.33 1
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs10074991
PRKAA1
0.851 0.120 5 40790449 intron variant G/A snv 0.31 3
rs10077591 1.000 0.040 5 165935005 intergenic variant C/T snv 0.44 1
rs1008078 1.000 0.040 1 90724174 non coding transcript exon variant C/T snv 0.33 2
rs10083370
LINC00637 ; PPP1R13B
1.000 0.040 14 103847845 intron variant G/A snv 0.55 1
rs10085567
GTF2IP7
1.000 0.040 7 76104888 intron variant A/C snv 0.43 1
rs10098073
TSNARE1
1.000 0.040 8 142228143 intron variant C/A snv 0.35 1
rs10124101
LOC102724322
1.000 0.040 9 36308830 upstream gene variant G/A snv 0.53 1
rs10135277 1.000 0.040 14 35354025 TF binding site variant C/T snv 0.43 1
rs10140896
EML5
1.000 0.040 14 88752194 intron variant C/A;G;T snv 1
rs10148671
LINC02326
1.000 0.040 14 29000167 intron variant T/C snv 0.51 1
rs10155413
LINC02511
1.000 0.040 4 137116128 intron variant T/C snv 0.35 1
rs10156310
NSD3
1.000 0.040 8 38351611 intron variant A/C;G;T snv 1
rs10180106
CTNNA2
1.000 0.040 2 79994772 intron variant G/A snv 0.22 1
rs10196799
ZNF804A
1.000 0.040 2 184776001 intron variant A/T snv 0.34 1
rs10199182
LINC01830 ; LINC01884
1.000 0.040 2 22524252 intron variant A/G;T snv 1
rs10204454 1.000 0.040 2 193481559 intergenic variant C/T snv 0.44 1
rs10204933 1.000 0.040 2 228206898 intergenic variant A/G snv 0.15 1