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: rs1114167298
rs1114167298
5 0.882 0.120 3 6861849 missense variant T/C snv 7.0E-06 0.700 0
dbSNP: rs1114167300
rs1114167300
6 0.925 0.040 3 7578878 missense variant C/T snv 0.700 0
dbSNP: rs1114167301
rs1114167301
6 0.925 0.040 3 7578930 missense variant C/A;T snv 4.0E-06 0.700 0