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: rs374450077
rs374450077
1 1.000 0.040 7 154769497 missense variant C/T snv 8.8E-05 2.4E-04 0.010 1.000 1 2016 2016