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: rs144610914
rs144610914
3 0.882 0.240 13 72908550 missense variant A/G snv 5.8E-05 2.1E-05 0.700 0
dbSNP: rs911707459
rs911707459
2 0.925 0.120 13 72965358 missense variant A/T snv 7.0E-06 0.700 0
dbSNP: rs10786691
rs10786691
3 0.925 0.160 10 102604895 intron variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs202676
rs202676
7 0.851 0.160 11 49206068 stop lost A/G snv 0.28 0.33 0.010 1.000 1 2012 2012
dbSNP: rs2486668
rs2486668
6 0.807 0.320 1 24331573 missense variant C/G snv 0.16 0.17 0.010 1.000 1 2019 2019
dbSNP: rs34396413
rs34396413
3 0.925 0.160 6 10400802 intron variant AGA/- delins 6.8E-02 6.9E-02 0.010 1.000 1 2019 2019