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: rs2612091
rs2612091
3 0.882 0.160 18 683607 intron variant C/T snv 0.63 0.010 1.000 1 2015 2015
dbSNP: rs2741171
rs2741171
1 1.000 0.080 18 700687 intron variant T/C;G snv 0.010 1.000 1 2015 2015