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: rs1296969984
rs1296969984
3 0.882 0.240 8 142876243 missense variant T/G snv 0.010 1.000 1 2005 2005
dbSNP: rs1447069098
rs1447069098
3 0.882 0.240 8 142874997 missense variant C/T snv 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs374517238
rs374517238
1 1.000 0.040 8 142874434 missense variant A/T snv 9.9E-04 3.5E-04 0.010 1.000 1 2016 2016
dbSNP: rs387907572
rs387907572
4 0.851 0.240 8 142876278 missense variant G/A snv 7.0E-06 0.010 1.000 1 2005 2005