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: rs1339374391
rs1339374391
1 1 156135973 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs58327533
rs58327533
3 1.000 0.120 1 156114991 missense variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs60682848
rs60682848
8 0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 0.010 1.000 1 2001 2001