Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 10
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs7394579
FADS2 ; FADS1
1.000 0.080 11 61813978 intron variant A/G snv 0.22 5
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 5
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs10886430
GRK5
10 119250744 intron variant A/G snv 8.8E-02 3
rs17116384
ZBTB16
11 114110519 intron variant A/G snv 0.25 3
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 3
rs2157770
LOC100130548 ; BRD3
9 134056342 intron variant A/G snv 0.33 3
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25 3
rs10220411
ACTN1-AS1
14 68985371 intron variant A/G snv 0.29 2
rs11121012
CAMTA1
1 7734229 intron variant A/G snv 0.62 2
rs12820906
PITPNM2
12 123008576 intron variant A/G snv 0.20 2
rs151361
PRELID3B ; SLMO2-ATP5E
20 59038947 intron variant A/G snv 0.24 2
rs2227831
F2R
5 76727669 intron variant A/G snv 2.7E-02 2
rs59508494
TPM4
19 16100820 non coding transcript exon variant A/G snv 5.1E-02 2
rs7585866 2 191831529 downstream gene variant A/G snv 0.24 2
rs9473147 6 47641856 regulatory region variant A/G snv 0.27 2
rs9660992
TMCC2
1 205280322 intron variant A/G snv 0.43 2
rs117107187
ITGB3
17 47252031 upstream gene variant A/G snv 5.5E-03 1
rs12485738
ARHGEF3
3 56831748 intron variant A/G snv 0.63 1
rs12589699
LOC107984647
14 68746168 intergenic variant A/G snv 0.15 1
rs160189
LOC107985162 ; NFATC1
18 79472709 intron variant A/G snv 0.41 1