Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs211234
KL
1.000 0.040 13 33020990 intron variant G/A;C snv 1
rs211239
KL
1.000 0.040 13 33022051 intron variant A/G;T snv 1