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: rs679620
rs679620
17 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 0.030 1.000 3 2009 2019
dbSNP: rs591058
rs591058
3 0.882 0.160 11 102840607 intron variant T/C snv 0.58 0.57 0.020 1.000 2 2009 2017
dbSNP: rs650108
rs650108
6 0.827 0.160 11 102838056 intron variant G/A snv 0.31 0.020 1.000 2 2009 2017
dbSNP: rs3025058
rs3025058
26 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 0.010 1.000 1 2017 2017