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: rs138623341
rs138623341
1 1.000 0.080 9 136859975 missense variant C/T snv 1.9E-03 2.0E-03 0.700 0
dbSNP: rs755530502
rs755530502
1 1.000 0.080 9 136854270 missense variant C/A snv 5.4E-05 5.6E-05 0.700 0