Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104894831
rs104894831
1.000 0.160 X 101407786 missense variant G/A snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.810 1.000 6 1989 2017
dbSNP: rs398123201
rs398123201
1.000 0.160 X 101407779 missense variant A/G snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.800 1.000 5 1989 2017
dbSNP: rs1555987232
rs1555987232
1.000 0.160 X 101407902 start lost A/G snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 1.000 4 1997 2017
dbSNP: rs104894835
rs104894835
1.000 0.160 X 101407803 missense variant T/C snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.800 1.000 3 1989 2017
dbSNP: rs398123199
rs398123199
1.000 0.160 X 101407785 missense variant G/A;C snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 1.000 3 2000 2016
dbSNP: rs1555987101
rs1555987101
1.000 0.160 X 101407763 missense variant C/G snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 1.000 2 2001 2017
dbSNP: rs1555987215
rs1555987215
1.000 0.160 X 101407878 frameshift variant T/- del
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 1.000 2 2000 2005
dbSNP: rs1569306181
rs1569306181
1.000 0.160 X 101407818 frameshift variant -/C delins
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 1.000 2 2001 2008
dbSNP: rs869312134
rs869312134
1.000 0.160 X 101407845 missense variant G/T snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.800 1.000 1 2016 2016
dbSNP: rs869312135
rs869312135
1.000 0.160 X 101407842 missense variant A/G snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.800 1.000 1 2016 2016
dbSNP: rs869312136
rs869312136
1.000 0.160 X 101407806 missense variant T/C snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.800 1.000 1 2016 2016
dbSNP: rs869312137
rs869312137
1.000 0.160 X 101407800 missense variant C/T snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.800 1.000 1 2016 2016
dbSNP: rs869312138
rs869312138
1.000 0.160 X 101407797 missense variant A/C snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.800 1.000 1 2016 2016
dbSNP: rs869312139
rs869312139
1.000 0.160 X 101407714 missense variant T/A snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.800 1.000 1 2002 2017
dbSNP: rs869312226
rs869312226
1.000 0.160 X 101407795 missense variant C/G;T snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 1.000 1 2007 2007
dbSNP: rs104894829
rs104894829
1.000 0.160 X 101407773 stop gained C/T snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 0
dbSNP: rs104894836
rs104894836
1.000 0.160 X 101407738 missense variant A/C snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.800 1.000 0 1989 2017
dbSNP: rs104894848
rs104894848
1.000 0.160 X 101407710 missense variant C/G snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.820 1.000 0 1989 2017
dbSNP: rs1555987175
rs1555987175
1.000 0.160 X 101407831 frameshift variant -/ACGAGGGCCAGGAA delins
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 0
dbSNP: rs797044613
rs797044613
1.000 0.160 X 101407780 missense variant T/C;G snv 9.4E-06
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.810 1.000 0 2002 2017
dbSNP: rs869312316
rs869312316
1.000 0.160 X 101407850 frameshift variant AAGCG/- delins
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.700 0
dbSNP: rs104894828
rs104894828
0.882 0.160 X 101398467 missense variant C/A;T snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.840 1.000 20 1989 2019
dbSNP: rs104894845
rs104894845
0.807 0.160 X 101401752 missense variant C/G;T snv 5.5E-04
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.860 1.000 18 1989 2018
dbSNP: rs28935197
rs28935197
0.776 0.280 X 101398942 missense variant T/C snv 5.5E-06
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.860 1.000 18 1989 2018
dbSNP: rs104894827
rs104894827
1.000 0.160 X 101398033 missense variant G/A snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease
0.800 1.000 14 1989 2017