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: rs1214110864
rs1214110864
2 1.000 0.040 7 87408071 missense variant A/T snv 0.010 1.000 1 2007 2007
dbSNP: rs2230028
rs2230028
5 0.827 0.080 7 87426860 missense variant T/C;G snv 1.0E-01 0.010 1.000 1 2009 2009
dbSNP: rs72552778
rs72552778
5 0.827 0.040 7 87447080 missense variant G/A snv 1.6E-04 1.7E-04 0.010 1.000 1 2014 2014