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: rs3824660
rs3824660
1 1.000 0.120 10 8062759 intron variant C/T snv 0.49 0.800 1.000 2 2014 2019
dbSNP: rs2275806
rs2275806
1 1.000 0.120 10 8053377 non coding transcript exon variant G/A snv 0.44 0.800 1.000 1 2012 2012
dbSNP: rs3781094
rs3781094
2 1.000 0.120 10 8059464 intron variant A/C snv 0.52 0.700 1.000 1 2015 2015