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: rs1105881
rs1105881
1 15 41780332 intron variant C/G snv 0.29 0.700 1.000 2 2018 2019
dbSNP: rs12440605
rs12440605
1 15 41810087 intron variant G/A snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs7175346
rs7175346
1 15 41808476 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019