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: rs371151471
rs371151471
1 1.000 0.040 6 52465092 missense variant C/T snv 1.2E-03 2.0E-04 0.700 1.000 7 2004 2017