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: rs16861990
rs16861990
2 1 169165889 intron variant A/C snv 5.5E-02 0.800 1.000 2 2011 2012
dbSNP: rs1208327
rs1208327
2 1 169327626 intron variant C/G;T snv 0.700 1.000 2 2011 2012
dbSNP: rs1209731
rs1209731
2 1 169355555 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs2040445
rs2040445
1 1 169247174 intron variant C/G;T snv 0.700 1.000 1 2019 2019