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: rs9416703
rs9416703
1 10 58523248 intron variant A/C snv 0.46 0.700 1.000 2 2018 2019
dbSNP: rs1649078
rs1649078
1 10 58533560 intron variant A/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs7392584
rs7392584
1 10 58523330 intron variant C/G;T snv 0.700 1.000 1 2019 2019