Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs583522
WAKMAR2 ; TNFAIP3
0.925 0.080 6 137868747 intron variant C/A;T snv 3
rs7436
COL6A3
0.925 0.080 2 237324168 3 prime UTR variant T/A snv 0.10 3
rs748676559
ACACA
0.925 0.080 17 37284932 missense variant C/T snv 4.0E-06 2.1E-05 3
rs750408412
CYP2E1
0.925 0.080 10 133538938 missense variant A/G snv 3
rs753225272
FAT4
0.925 0.080 4 125491730 missense variant C/G;T snv 8.0E-06; 4.0E-06 3
rs770728618
IL17D
0.925 0.080 13 20721723 missense variant G/C;T snv 5.3E-05 3
rs776933870
PLCE1
0.925 0.080 10 94306632 missense variant A/G snv 8.0E-06 3
rs886063150
CA2
0.925 0.080 8 85477151 missense variant C/A;T snv 8.0E-06 3
rs917870680
MDM2
0.925 0.080 12 68839304 missense variant A/G snv 3
rs10058728
CSNK1A1
1.000 0.080 5 149524529 intron variant A/T snv 0.64 2
rs6772209 1.000 0.080 3 175929377 intergenic variant G/A snv 4.1E-02 2
rs8030672 1.000 0.080 15 68766745 intergenic variant T/A snv 5.4E-02 2
rs9868873
SEMA5B
1.000 0.080 3 123012063 intron variant G/A snv 0.28 2
rs10002268 1.000 0.080 4 55653725 intergenic variant T/C snv 0.41 1
rs10786161
NOC3L
1.000 0.080 10 94347914 intron variant C/T snv 0.31 1
rs10821515
SYK
1.000 0.080 9 90862614 intron variant G/A;C snv 1
rs10882424
PLCE1 ; NOC3L
1.000 0.080 10 94326321 intron variant T/G snv 0.31 1
rs10882430
NOC3L ; PLCE1
1.000 0.080 10 94330915 3 prime UTR variant A/G snv 0.31 1
rs11066008
ACAD10
1.000 0.080 12 111702865 intron variant A/G snv 9.1E-03 1
rs11184738
LOC105378885
1.000 0.080 1 106056773 intron variant G/A snv 7.3E-02 1
rs11187844
PLCE1
1.000 0.080 10 94296872 intron variant C/A snv 0.12 1
rs11187853
PLCE1
1.000 0.080 10 94312471 intron variant G/A;C snv 1
rs11187876
NOC3L ; PLCE1
1.000 0.080 10 94330382 3 prime UTR variant C/T snv 0.31 1
rs11265282
LOC105371464 ; FCRL6
1.000 0.080 1 159804618 intron variant T/C snv 0.26 1
rs11934363
SLC2A9
1.000 0.080 4 9910477 intron variant A/G snv 0.24 1