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: rs2231495
rs2231495
1 22 17188416 missense variant T/A;C;G snv 8.0E-06; 0.34; 1.2E-05 0.700 1.000 2 2018 2018
dbSNP: rs2041144
rs2041144
1 22 17242284 intron variant C/A;G snv 0.700 1.000 1 2018 2018