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: rs104894654
rs104894654
2 0.925 0.080 18 34794250 missense variant C/T snv 1.6E-05 2.1E-05 0.800 1.000 1 2001 2001
dbSNP: rs775975702
rs775975702
2 0.925 0.120 18 34766039 missense variant A/G snv 4.0E-06 7.0E-06 0.700 0