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: rs1378942
rs1378942
CSK
16 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 5 2009 2018
dbSNP: rs1350193
rs1350193
CSK
2 15 74791940 intron variant G/C snv 0.67 0.700 1.000 1 2018 2018