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: rs2056202
rs2056202
4 0.882 0.040 2 171855970 intron variant T/C snv 0.81 0.77 0.040 1.000 4 2005 2010
dbSNP: rs2292813
rs2292813
3 0.882 0.040 2 171787719 intron variant T/C snv 0.81 0.040 1.000 4 2005 2010