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: rs104893941
rs104893941
11 0.756 0.214 5 179836445 missense variant C/T snp 9.8E-04 4.1E-04 0.010 1.000 1 2011 2011
dbSNP: rs72656351
rs72656351
2 1.000 0.107 17 50185576 missense variant C/T snp 0.010 1.000 1 2002 2002
dbSNP: rs758272654
rs758272654
28 0.667 0.536 20 58909201 synonymous variant T/C snp 4.0E-06 0.010 1.000 1 2008 2008