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: rs1558162
rs1558162
2 1.000 0.040 7 39471024 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs3937443
rs3937443
2 1.000 0.040 7 39474399 intron variant T/C snv 0.77 0.700 1.000 1 2019 2019