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: rs2062305
rs2062305
2 1.000 0.040 13 42478744 intron variant G/A snv 0.46 0.800 1.000 2 2010 2017
dbSNP: rs80244186
rs80244186
1 1.000 0.040 13 42343725 intron variant T/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs9525625
rs9525625
2 1.000 0.040 13 42443894 intron variant T/C snv 0.45 0.700 1.000 1 2015 2015