Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1002658 1.000 0.120 6 137660447 intron variant C/T snv 0.15 1
rs3093998 1.000 0.120 6 31517397 downstream gene variant C/A snv 0.70 1
rs3130237 1.000 0.120 6 33129784 downstream gene variant T/C snv 0.13 1
rs6565176 1.000 0.120 16 30163605 intergenic variant T/A;C snv 1
rs9267947 1.000 0.120 6 32243441 intergenic variant A/G;T snv 1
rs9482849 1.000 0.120 6 127967391 downstream gene variant T/C snv 0.14 1
rs2240064
CCHCR1
1.000 0.120 6 31146796 intron variant G/A;T snv 1
rs2855430
COL11A2
1.000 0.120 6 33173503 missense variant G/A snv 0.12 9.9E-02 1
rs1244186
GATA3-AS1 ; GATA3
1.000 0.120 10 8050720 non coding transcript exon variant T/A;C snv 1
rs485411
GATA3-AS1 ; GATA3
1.000 0.120 10 8051222 non coding transcript exon variant T/A;C;G snv 0.81 1
rs501764
GATA3-AS1 ; GATA3
1.000 0.120 10 8051071 non coding transcript exon variant G/T snv 0.87 0.86 1
rs387906223
KLHDC8B
1.000 0.120 3 49171662 5 prime UTR variant C/T snv 4.8E-03 1
rs1432295
LINC01185
1.000 0.120 2 60839531 intron variant G/A snv 0.69 1
rs6439924
LOC105374132 ; CLSTN2
1.000 0.120 3 140450815 intron variant A/C snv 0.21 1
rs805286
LY6G6E ; LY6G6D ; LY6G6F-LY6G6D
1.000 0.120 6 31711530 intron variant A/G snv 0.42 1
rs2523710
MICB-DT
1.000 0.120 6 31483132 intron variant G/A snv 0.14 1
rs7111520
POU2AF1
1.000 0.120 11 111378886 intron variant G/A snv 0.58 1
rs2608053
PVT1
1.000 0.120 8 128063586 intron variant T/C snv 0.50 1
rs4733809
PVT1
1.000 0.120 8 127977046 intron variant C/T snv 0.54 1
rs752427
PVT1
1.000 0.120 8 127967762 intron variant C/T snv 0.55 1
rs2069757
TH2LCRR
1.000 0.120 5 132662721 intron variant G/A snv 7.5E-02 1
rs13195441 0.925 0.200 6 32775521 intergenic variant G/A snv 0.30 2
rs181997 0.925 0.160 6 32932941 downstream gene variant G/A;C snv 2
rs3129214 0.925 0.160 6 33149481 downstream gene variant C/T snv 0.24 2
rs4959089 0.925 0.200 6 32251948 upstream gene variant A/G snv 0.22 2