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: rs441460
rs441460
1 6 25548060 intron variant G/A snv 0.45 0.800 1.000 1 2011 2011
dbSNP: rs12526480
rs12526480
2 6 25533306 intron variant T/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs214053
rs214053
2 6 25527735 intron variant T/C snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs926326
rs926326
1 6 25575174 intron variant A/C;G snv 0.700 1.000 1 2016 2016