Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12373168
MAPT-AS1 ; SPPL2C
1.000 0.080 17 45846971 3 prime UTR variant A/C snv 0.16 0.20 2
rs1331308
HBS1L
6 135083984 intron variant A/C snv 0.61 2
rs17564983
LOC105371800 ; MAPT
1.000 0.040 17 45934459 intron variant A/C snv 0.14 2
rs17574040
MAPT
1.000 0.080 17 46025499 3 prime UTR variant A/C snv 0.14 2
rs199529
LRRC37A2
17 46759851 downstream gene variant A/C snv 0.25 2
rs2026310 6 135144413 intergenic variant A/C snv 0.27 2
rs2076538
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32349694 non coding transcript exon variant A/C snv 0.42 0.33 2
rs2157152 22 37009870 upstream gene variant A/C snv 0.62 2
rs2158257
MAPT ; KANSL1
1.000 0.080 17 46026977 3 prime UTR variant A/C snv 0.14 2
rs2239063
CACNA1C
1.000 0.040 12 2402665 intron variant A/C snv 0.23 2
rs241036
LINC02210 ; LINC02210-CRHR1
17 45654353 non coding transcript exon variant A/C snv 0.14 2
rs243079
MIR4432HG ; MIR4432
2 60387893 intron variant A/C snv 0.42 2
rs2942202
SLC25A37
8 23560931 intron variant A/C snv 0.53 2
rs3893275
LOC105374303
3 196192085 regulatory region variant A/C snv 0.13 2
rs518374
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32297933 intron variant A/C snv 0.33 2
rs552965964
MAPT
1.000 0.080 17 45987393 intron variant A/C snv 2
rs566628150
KANSL1
1.000 0.080 17 46182173 intron variant A/C snv 2
rs571568457
KANSL1
1.000 0.080 17 46171730 synonymous variant A/C snv 2
rs7197756 16 68241613 upstream gene variant A/C snv 0.27 2
rs9379851 6 26354552 regulatory region variant A/C snv 7.6E-02 2
rs1010549 6 164071351 intergenic variant A/C snv 0.50 1
rs10514898
KANSL1
17 46042270 non coding transcript exon variant A/C snv 0.14 1
rs11713316 3 142260277 intergenic variant A/C snv 0.51 1
rs1175549
SMIM1
1 3775163 intron variant A/C snv 0.32 1
rs11759062
HBS1L
6 135060110 intron variant A/C snv 0.31 1