Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10211550
MOB4 ; HSPE1-MOB4
1.000 0.040 2 197518575 intron variant G/T snv 0.37 2
rs1021487 1.000 0.040 4 58590920 intergenic variant T/C snv 0.15 1
rs10226475
MAD1L1
1.000 0.040 7 2186527 intron variant A/G snv 0.34 1
rs1023500
CENPM
1.000 0.040 22 41944840 intron variant T/C snv 0.27 1
rs1024582
CACNA1C
1.000 0.040 12 2293080 intron variant A/G;T snv 2
rs1025641
C10orf90
1.000 0.040 10 126618623 intron variant T/C snv 0.43 1
rs10272006
SP4
0.925 0.080 7 21480514 intron variant G/A snv 0.75 2
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs10277664
TBXAS1
1.000 0.040 7 139806781 intron variant C/T snv 0.36 1
rs1033023 1.000 0.040 1 239045834 intergenic variant T/A snv 0.36 1
rs1033394
HDAC2-AS2 ; LOC107986638
1.000 0.040 6 114392159 intron variant C/T snv 0.77 1
rs1035130
IL18R1
1.000 0.040 2 102384942 synonymous variant C/T snv 0.26 0.24 1
rs1035578
SNX29
1.000 0.040 16 12437508 intron variant G/A snv 0.57 2
rs10399805
CHI3L1
0.851 0.240 1 203186870 upstream gene variant G/A;T snv 1
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 5
rs10425465
PEPD
1.000 0.040 19 33407028 intron variant T/G snv 0.34 1
rs1042779
ITIH1
0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 3
rs1042992
BNIP3L
1.000 0.040 8 26411675 3 prime UTR variant C/T snv 0.19 1
rs10429924 1.000 0.040 1 244227262 intergenic variant C/T snv 8.8E-02 1
rs1046778
AS3MT ; BORCS7-ASMT ; LOC107984265
0.851 0.160 10 102901727 3 prime UTR variant T/C snv 0.30 1
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 4
rs10489202
MPC2
0.925 0.080 1 167933841 intron variant G/T snv 0.20 2
rs10490175
NRXN1
1.000 0.040 2 50855616 intron variant G/A snv 0.16 2
rs10498146 1.000 0.040 2 222987318 intergenic variant A/G snv 6.2E-02 1