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: rs1211375
rs1211375
4 1.000 0.040 16 190281 intron variant A/C;T snv 0.800 1.000 2 2013 2017
dbSNP: rs111775488
rs111775488
2 16 192899 intron variant G/C snv 5.8E-02 7.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs1211377
rs1211377
1 16 207157 intron variant C/A snv 0.52 0.700 1.000 1 2018 2018