Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11038167 1.000 0.040 11 44821583 intron variant A/C;G snv 1
rs11038172 1.000 0.040 11 44834046 intron variant A/G snv 5.1E-02 1
rs835784 1.000 0.040 11 44842267 intron variant A/G snv 0.52 1