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: rs10965235
rs10965235
1 1.000 0.040 9 22115106 intron variant C/A snv 0.15 0.820 1.000 2 2010 2014
dbSNP: rs10757272
rs10757272
6 0.851 0.160 9 22088261 intron variant C/T snv 0.41 0.700 1.000 1 2017 2017