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: rs153662
rs153662
1 5 142432041 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs250100
rs250100
1 5 142605814 intron variant T/C snv 0.90 0.700 1.000 1 2019 2019
dbSNP: rs34427173
rs34427173
1 5 142328625 intron variant C/- delins 0.27 0.700 1.000 1 2019 2019