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: rs1045433
rs1045433
1 1.000 0.160 3 3149742 non coding transcript exon variant T/C snv 0.15 0.010 1.000 1 2016 2016
dbSNP: rs1672753
rs1672753
4 0.882 0.240 3 3179746 upstream gene variant C/T snv 0.71 0.010 1.000 1 2019 2019
dbSNP: rs6768972
rs6768972
2 1.000 0.160 3 3180101 upstream gene variant A/C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs711613
rs711613
1 1.000 0.160 3 3178805 intron variant T/C snv 0.51 0.010 1.000 1 2016 2016