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: rs17848368
rs17848368
1 1.000 11 74006298 missense variant G/A snv 1.1E-04 7.0E-05 0.700 0
dbSNP: rs2229707
rs2229707
2 0.925 0.080 11 74006202 missense variant C/T snv 1.0E-02 3.9E-02 0.700 0