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: rs369576054
rs369576054
6 0.807 0.120 4 85994925 missense variant C/T snv 2.8E-05 4.9E-05 0.010 1.000 1 2001 2001
dbSNP: rs377522479
rs377522479
4 0.882 0.080 4 85931021 missense variant C/T snv 2.0E-05 3.5E-05 0.010 < 0.001 1 2001 2001
dbSNP: rs771723690
rs771723690
3 0.882 0.080 4 85570622 synonymous variant G/A snv 1.6E-05 0.010 < 0.001 1 2001 2001