Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2883821
IGSF21
1.000 1 18240357 intron variant C/A;T snv 5
rs35290534 1.000 4 187219164 regulatory region variant T/C snv 0.43 5
rs61433759
LINC01150
1.000 11 1897978 intron variant T/G snv 7.7E-02 5
rs859208
AKR7A2
1.000 1 19308470 missense variant C/G snv 2.8E-02 8.6E-02 5
rs548853
NCBP2 ; NCBP2AS2 ; NCBP2-AS1
1.000 3 196941488 splice region variant C/A;T snv 0.53 5
rs61998208
ZNF90
1.000 19 20118360 missense variant C/T snv 1.0E-02 7.5E-02 5
rs12532102
CDCA7L
1.000 7 21927090 intron variant A/G snv 0.82 5
rs7697101 1.000 4 22173148 intron variant T/C snv 0.59 5
rs6576462
MKRN3
1.000 15 23569519 non coding transcript exon variant C/T snv 0.93 5
rs429360
PLD5
1.000 1 242242264 intron variant T/A;C snv 5
rs113974007 1.000 1 244750932 intergenic variant T/C snv 7.3E-02 5
rs74654316
DNAJC27
1.000 2 24946443 3 prime UTR variant G/A snv 9.4E-02 5
rs2505447
LINC00836
1.000 10 25728984 intron variant A/G;T snv 5
rs9975780 1.000 21 26678731 intergenic variant C/T snv 0.10 5
rs217514
CREB5
1.000 7 28506192 intron variant T/C snv 0.27 5
rs4287603
RAP1GAP2
1.000 17 2872448 intron variant G/A snv 0.36 5
rs10182825
PPP1CB ; SPDYA
1.000 2 28788221 intron variant G/A snv 9.0E-02 5
rs3131103
TRIM27
1.000 6 28925757 upstream gene variant C/G;T snv 5
rs11933652 1.000 4 28961215 intergenic variant T/C snv 0.12 5
rs6731759
ALK
1.000 2 29804123 intron variant A/G snv 0.42 5
rs72847487 1.000 3 30504455 regulatory region variant C/T snv 9.0E-02 5
rs57989216 1.000 6 31368014 intron variant G/A snv 3.2E-02 5
rs57541735
TSSK3 ; FAM229A
1.000 1 32362000 missense variant G/A;C snv 4.6E-03 5
rs7250377 1.000 19 32543335 intergenic variant G/T snv 9.9E-02 5
rs9688730 1.000 6 33957119 intergenic variant A/C snv 6.5E-02 5