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: rs786205680
rs786205680
1 1.000 0.160 5 132934293 missense variant G/A snv 0.800 1.000 1 2015 2015
dbSNP: rs786205233
rs786205233
1 1.000 0.160 5 132934305 missense variant T/C snv 0.800 0
dbSNP: rs786205679
rs786205679
1 1.000 0.160 5 132934304 missense variant G/C snv 0.800 0