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: rs10477176
rs10477176
1 5 142410760 intron variant A/G snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs1650911
rs1650911
1 5 142361055 intron variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs3853476
rs3853476
2 5 142438189 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs76271629
rs76271629
1 5 142348405 intron variant G/A snv 0.18 0.700 1.000 1 2019 2019