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: rs1057516030
rs1057516030
14 0.807 0.280 21 37480785 stop gained -/A delins 0.700 0
dbSNP: rs121908247
rs121908247
5 0.851 0.160 19 13235693 missense variant C/T snv 0.700 0
dbSNP: rs797045277
rs797045277
5 0.882 0.280 6 157198907 splice region variant G/A snv 0.700 0
dbSNP: rs869312685
rs869312685
11 0.807 0.240 3 4815135 missense variant G/A;C snv 0.700 0