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: rs80356733
rs80356733
7 0.790 0.200 1 11022451 missense variant G/T snv 0.010 1.000 1 2008 2008
dbSNP: rs80356734
rs80356734
4 0.851 0.160 1 11022464 missense variant A/G snv 0.010 1.000 1 2008 2008