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: rs544557652
rs544557652
1 1.000 0.080 4 174975617 missense variant C/T snv 1.0E-04 9.1E-05 0.700 0
dbSNP: rs772388824
rs772388824
1 1.000 0.080 4 174976138 missense variant G/A snv 1.2E-05 7.0E-06 0.700 0