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: rs1598856
rs1598856
1 1.000 0.080 4 102524958 intron variant A/G snv 0.61 0.700 1.000 1 2017 2017
dbSNP: rs230534
rs230534
3 0.882 0.120 4 102527884 intron variant T/C snv 0.73 0.700 1.000 1 2017 2017