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: rs13043926
rs13043926
2 20 33832650 intron variant G/C snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs2747539
rs2747539
2 20 33830562 intron variant C/T snv 0.15 0.700 1.000 1 2010 2010
dbSNP: rs4911368
rs4911368
2 20 33833936 intron variant G/A snv 0.15 0.700 1.000 1 2010 2010
dbSNP: rs6087528
rs6087528
2 20 33823138 intron variant T/A snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs6088314
rs6088314
2 20 33836254 intron variant T/C snv 0.10 0.700 1.000 1 2010 2010