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: rs1254341668
rs1254341668
1 6 15523111 missense variant G/A snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs2619528
rs2619528
2 1.000 0.040 6 15649598 intron variant C/T snv 0.26 0.010 1.000 1 2010 2010