Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1046321
PEX12
17 35575265 3 prime UTR variant T/C snv 0.38 2
rs10479001
P4HA2 ; PDLIM4
5 132272028 missense variant C/T snv 4.6E-02 7.2E-02 2
rs1047912
DIP2B
12 50745079 3 prime UTR variant C/T snv 0.21 3
rs10483353
AP4S1
14 31083414 intron variant T/C snv 5.4E-02 0.11 2
rs10503728
SLC25A37
8 23563489 intron variant A/C;G snv 2
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 8
rs10511434
SMARCA2
9 2114024 intron variant T/C snv 0.14 2
rs10516140
SQSTM1
5 179813910 intron variant A/C snv 0.76 2
rs1064807
SDAD1P1
8 26379462 non coding transcript exon variant C/T snv 0.71 2
rs10710560
MXD1
2 69925927 intron variant T/- delins 9.0E-02 2
rs10739069
RCL1
9 4863305 intron variant T/A snv 0.25 2
rs10741688
SOX6
11 15990568 intron variant A/C;T snv 0.51 2
rs10755927
LOC105375746
8 125617350 intergenic variant C/T snv 0.36 2
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs10774463
WNK1
12 792399 intron variant G/A;C snv 2
rs10801851
HFM1
1 91281449 intron variant C/T snv 0.48 2
rs10815095
RCL1 ; MIR101-2
9 4848297 intron variant A/G snv 0.19 4
rs10821339
LOC105376154 ; NUTM2F
9 94324185 intron variant G/A snv 0.28 2
rs10844074
RESF1
12 31966182 intron variant T/C snv 0.15 2
rs10846305
LOC101928362
12 16157882 regulatory region variant A/G snv 0.30 2
rs10872447
LOC101928373 ; PDE7B
6 135883367 non coding transcript exon variant A/G snv 0.45 2
rs10876169
SLC4A8 ; GALNT6
12 51389636 intron variant T/A;C snv 2
rs10883353 10 99496351 intergenic variant G/A snv 0.82 2
rs10897221 11 62171647 downstream gene variant G/T snv 0.22 2
rs10898438 11 86147211 intergenic variant G/A;C snv 2