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: rs397516165
rs397516165
4 0.925 0.080 14 23424118 missense variant C/G;T snv 0.700 0
dbSNP: rs727504237
rs727504237
3 0.882 0.080 14 23428529 missense variant G/T snv 0.700 0
dbSNP: rs3218716
rs3218716
17 0.716 0.280 14 23425316 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 0.700 0