Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12325410
LOC101927026
0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
rs7219021
TTLL6
0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs76371172
OTUD7A ; LOC105370753
0.882 0.040 15 31522252 intron variant T/G snv 9.1E-03 4
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 3
rs4721295
MAD1L1
0.882 0.040 7 1997034 intron variant T/G snv 0.33 3
rs11647445
GRIN2A
0.925 0.040 16 9833109 intron variant T/G snv 0.35 2
rs2273684
GSS
1.000 0.040 20 34941963 intron variant T/G snv 0.52 2
rs6088662
MYH7B
1.000 0.040 20 34959830 intron variant T/G snv 0.20 2
rs6550435
LINC02033
0.925 0.040 3 36822998 upstream gene variant T/G snv 0.38 2
rs79403677
FAM177A1
0.925 0.040 14 35069925 intron variant T/G snv 0.17 2
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 2
rs10821745
ANK3
1.000 0.040 10 60376448 intron variant T/G snv 9.7E-02 1
rs10889182
LINC01748
1.000 0.040 1 60532523 intron variant T/G snv 0.33 1
rs142643109 1.000 0.040 17 62310560 intergenic variant T/G snv 1.0E-02 1
rs1477143 1.000 0.040 17 55258467 intergenic variant T/G snv 0.76 1
rs1532965
LINC02033
1.000 0.040 3 36819705 intron variant T/G snv 0.37 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs184148144 1.000 0.040 4 48443799 intergenic variant T/G snv 0.17 1
rs56361249
LMAN2L
1.000 0.040 2 96714492 intron variant T/G snv 0.28 1
rs62433108
DCBLD1
1.000 0.040 6 117483634 intron variant T/G snv 0.28 1
rs7108878
TENM4
1.000 0.040 11 79396763 intron variant T/G snv 0.10 1
rs7560357
MGAT4A
1.000 0.040 2 98631357 intron variant T/G snv 0.18 1
rs7652808
CADM2
1.000 0.040 3 85554493 intron variant T/G snv 0.70 1
rs9633553
LOC107984292 ; ANK3
1.000 0.040 10 60514979 intron variant T/G snv 8.3E-02 1
rs105633
DELE1 ; PCDH12
0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3