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: rs1078305
rs1078305
GSN
1 1.000 0.040 9 121289122 intron variant A/G snv 0.70 0.010 1.000 1 2016 2016
dbSNP: rs10818524
rs10818524
GSN
1 1.000 0.040 9 121267901 intron variant T/C snv 0.37 0.010 1.000 1 2016 2016