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: rs104894220
rs104894220
1 1.000 0.040 11 113416935 missense variant C/T snv 4.4E-05 6.3E-05 0.010 1.000 1 2000 2000