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: rs229541
rs229541
8 0.807 0.200 22 37195278 intron variant G/A snv 0.49 0.810 1.000 3 2008 2015
dbSNP: rs229526
rs229526
1 1.000 0.120 22 37185382 missense variant G/C;T snv 0.19; 4.0E-06 0.700 1.000 1 2011 2011
dbSNP: rs229533
rs229533
1 1.000 0.120 22 37191071 intron variant A/C snv 0.50 0.700 1.000 1 2015 2015