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: rs35449651
rs35449651
1 1.000 0.080 7 113878300 missense variant G/T snv 1.4E-03 1.5E-03 0.700 0
dbSNP: rs1799999
rs1799999
4 0.882 0.160 7 113878379 missense variant C/A snv 0.22 0.17 0.040 0.500 4 1998 2018