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: rs1056198
rs1056198
2 0.925 0.040 20 49939692 intron variant C/T snv 0.34 0.800 1.000 1 2012 2012
dbSNP: rs73129298
rs73129298
1 1.000 0.040 20 49949528 intron variant A/C snv 9.2E-02 0.700 1.000 1 2015 2015