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: rs4530754
rs4530754
3 5 123519722 intron variant G/A snv 0.61 0.800 1.000 3 2013 2018
dbSNP: rs58466006
rs58466006
1 5 123593271 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6595460
rs6595460
2 5 123572774 intron variant A/G snv 0.62 0.700 1.000 1 2018 2018