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: rs121912424
rs121912424
1 1.000 17 63930095 missense variant C/T snv 0.800 1.000 1 2007 2007
dbSNP: rs267606711
rs267606711
1 1.000 17 63930266 stop gained G/A snv 0.700 0