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: rs10824760
rs10824760
1 10 52665565 intron variant C/T snv 0.75 0.700 1.000 1 2018 2018
dbSNP: rs1159798
rs1159798
1 10 52652733 intron variant A/C snv 0.70 0.700 1.000 1 2018 2018
dbSNP: rs12258451
rs12258451
1 10 52664093 intron variant C/G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs1373004
rs1373004
2 10 52668065 intron variant T/G snv 0.75 0.700 1.000 1 2012 2012