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: rs1948915
rs1948915
1 1.000 0.160 8 127210176 intron variant T/C snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs16901979
rs16901979
17 0.724 0.480 8 127112671 intron variant C/A snv 0.16 0.010 1.000 1 2011 2011
dbSNP: rs2456449
rs2456449
5 0.827 0.280 8 127180736 intron variant A/G snv 0.30 0.010 1.000 1 2012 2012