Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12342421
JAK2 ; INSL6
0.851 0.080 9 5065750 intron variant G/C snv 0.23 5
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs17849241
SOCS3 ; LOC101928674
0.925 0.080 17 78358688 missense variant G/C;T snv 4.1E-06; 2.1E-04 3
rs12339666
INSL6 ; JAK2
0.925 0.080 9 5063296 intron variant G/T snv 0.34 3
rs10815148
JAK2 ; INSL6
0.882 0.080 9 5057284 intron variant T/A snv 0.33 3
rs3808850
JAK2
0.925 0.080 9 4983311 upstream gene variant T/A;C snv 2
rs2201862 0.925 0.080 3 168930251 downstream gene variant T/C snv 0.63 3
rs4495487
INSL6 ; JAK2
0.925 0.080 9 5072798 intron variant T/C snv 0.23 3
rs777342222
EGFR
1.000 0.080 7 55155925 missense variant T/C snv 4.0E-06 1
rs766642690
MPL
1.000 0.080 1 43352635 missense variant T/C;G snv 4.0E-06 1
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs11999802 1.000 0.080 9 5189773 upstream gene variant T/G snv 0.33 1
rs121913616
MPL
0.790 0.120 1 43349337 missense variant TG/AA mnv 8