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: rs751731391
rs751731391
1 1.000 0.080 10 121500901 missense variant C/T snv 1.2E-05 7.0E-06 0.010 1.000 1 2004 2004