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: rs62358361
rs62358361
C9
5 0.851 0.040 5 39327786 intron variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs34882957
rs34882957
C9
2 0.925 0.040 5 39331792 missense variant G/A snv 5.2E-03 6.1E-03 0.020 1.000 2 2018 2018
dbSNP: rs137891079
rs137891079
C9
1 1.000 0.040 5 39288783 missense variant C/T snv 5.9E-04 3.1E-04 0.010 1.000 1 2018 2018
dbSNP: rs147701327
rs147701327
C9
1 1.000 0.040 5 39341270 missense variant G/A snv 1.6E-04 2.0E-04 0.010 1.000 1 2018 2018