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: rs8056893
rs8056893
2 16 68270489 intron variant C/A;T snv 0.700 1.000 2 2016 2019
dbSNP: rs6499166
rs6499166
1 16 68293014 intron variant G/A snv 0.79 0.700 1.000 1 2012 2012
dbSNP: rs7185391
rs7185391
1 16 68289212 intron variant T/G snv 0.79 0.700 1.000 1 2019 2019
dbSNP: rs9888796
rs9888796
1 16 68263686 upstream gene variant T/C snv 0.80 0.700 1.000 1 2019 2019