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: rs104893823
rs104893823
5 0.882 0.040 3 52451285 missense variant C/T snv 0.010 1.000 1 2008 2008
dbSNP: rs267607123
rs267607123
4 0.882 0.080 3 52452222 missense variant A/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2008 2008