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: rs2071481
rs2071481
1 1.000 0.120 6 32852088 intron variant T/C snv 0.14 0.11 0.700 1.000 1 2007 2007
dbSNP: rs2071538
rs2071538
2 0.925 0.160 6 32850901 intron variant G/A snv 0.18 0.17 0.700 1.000 1 2007 2007
dbSNP: rs2071540
rs2071540
2 0.925 0.200 6 32845139 non coding transcript exon variant T/C snv 0.61 0.700 1.000 1 2007 2007