Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1006737
rs1006737
27 0.695 0.120 12 2236129 intron variant G/A snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs1024582
rs1024582
2 1.000 0.040 12 2293080 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2007044
rs2007044
6 0.882 0.040 12 2235794 intron variant A/G snv 0.50 0.700 1.000 1 2017 2017