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: rs7120118
rs7120118
2 0.716 0.360 11 47264739 intron variant T/C snv 0.38 0.800 1.000 1 2009 2012
dbSNP: rs10838681
rs10838681
3 1.000 0.040 11 47253513 intron variant G/A snv 0.34 0.700 1.000 1 2018 2018