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: rs750566714
rs750566714
1 1.000 0.040 22 37978082 missense variant C/T snv 7.0E-06 0.700 1.000 3 1999 2011