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: rs148319899
rs148319899
2 1.000 0.040 12 40346421 intron variant T/C snv 3.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs4768236
rs4768236
2 1.000 0.040 12 40362670 intron variant C/A;T snv 0.700 1.000 1 2015 2015