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: rs1553318
rs1553318
3 5 157052312 intron variant G/A;C snv 6.2E-03; 0.67 0.700 1.000 2 2015 2018
dbSNP: rs10066168
rs10066168
2 5 157057207 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs17573010
rs17573010
1 5 157050820 intron variant G/A snv 3.0E-02 0.700 1.000 1 2018 2018