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: rs1114167331
rs1114167331
1 1.000 0.040 10 110812301 missense variant C/G snv 0.700 0
dbSNP: rs267607003
rs267607003
3 0.925 0.040 10 110812310 missense variant C/A;G;T snv 0.700 0