Source: BEFREE ×
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: rs36053993
rs36053993
24 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 0.040 1.000 4 2012 2019
dbSNP: rs34612342
rs34612342
24 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.030 1.000 3 2012 2019