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: rs1420101
rs1420101
8 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 0.800 1.000 1 2009 2009
dbSNP: rs5833013
rs5833013
2 2 102352407 intron variant -/TA delins 0.700 1.000 1 2016 2016
dbSNP: rs6543119
rs6543119
1 2 102346612 intron variant A/T snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs9807989
rs9807989
2 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 0.700 1.000 1 2019 2019