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: rs1057520012
rs1057520012
1 1.000 0.040 4 65404419 missense variant C/T snv 0.800 1.000 1 2005 2005
dbSNP: rs199614818
rs199614818
1 1.000 0.040 4 65490529 missense variant C/A;T snv 4.0E-06; 2.4E-05 0.700 0