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: rs1933437
rs1933437
2 13 28050157 missense variant G/A snv 0.60 0.53 0.700 1.000 2 2018 2018
dbSNP: rs2504236
rs2504236
1 13 28039161 intron variant C/T snv 0.45 0.700 1.000 1 2015 2015
dbSNP: rs7318817
rs7318817
1 13 28043571 intron variant C/T snv 0.61 0.700 1.000 1 2019 2019
dbSNP: rs9507983
rs9507983
1 13 28045899 intron variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs9513018
rs9513018
1 13 28066426 intron variant G/A;T snv 0.700 1.000 1 2019 2019