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: rs2236313
rs2236313
1 1.000 0.040 6 166946901 intron variant T/C snv 0.53 0.50 0.800 1.000 1 2010 2010
dbSNP: rs2247314
rs2247314
1 1.000 0.040 6 166956742 intron variant T/C snv 0.42 0.700 1.000 1 2016 2016