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: rs373584770
rs373584770
5 0.827 0.120 11 105030337 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs781107669
rs781107669
1 1.000 0.080 11 105031227 missense variant C/T snv 8.0E-06 0.010 1.000 1 2004 2004