Source: CLINVAR

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: rs1553602498
rs1553602498
1.000 2 224497809 stop gained G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 25 1986 2016
dbSNP: rs1554770044
rs1554770044
1.000 9 137162182 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 25 1983 2017
dbSNP: rs1554770667
rs1554770667
0.882 9 137163845 missense variant C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 25 1983 2017
dbSNP: rs574622908
rs574622908
1.000 12 49046358 stop gained G/C;T snv 4.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 25 1988 2017
dbSNP: rs587783685
rs587783685
0.925 0.120 12 49032113 stop gained G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 25 1988 2017
dbSNP: rs587783690
rs587783690
0.925 0.120 12 49031255 stop gained G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 25 1988 2017
dbSNP: rs794727688
rs794727688
1.000 12 49026431 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 25 1988 2017
dbSNP: rs1555208063
rs1555208063
1.000 12 109800629 missense variant T/G snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 24 1976 2017
dbSNP: rs1553749681
rs1553749681
0.925 3 51064514 stop gained C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 23 2000 2018
dbSNP: rs1057521070
rs1057521070
0.925 0.200 18 55228999 missense variant C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 2007 2017
dbSNP: rs150800017
rs150800017
1.000 11 118489816 stop gained C/G;T snv 8.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1989 2017
dbSNP: rs1553630472
rs1553630472
1.000 3 41225721 stop gained C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1991 2017
dbSNP: rs1553631770
rs1553631770
1.000 3 41233398 missense variant A/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1991 2017
dbSNP: rs1555039343
rs1555039343
1.000 11 118481870 stop gained C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1989 2017
dbSNP: rs1555046404
rs1555046404
1.000 11 118503042 stop gained C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1989 2017
dbSNP: rs1555721921
rs1555721921
0.925 0.200 18 55234546 splice donor variant A/C;G snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 2007 2017
dbSNP: rs1555778204
rs1555778204
1.000 18 55261525 stop gained C/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 2007 2017
dbSNP: rs775104326
rs775104326
0.776 0.160 3 41224995 stop gained C/A;T snv 4.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1991 2017
dbSNP: rs781978013
rs781978013
1.000 11 118472681 stop gained G/A;T snv 4.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1989 2017
dbSNP: rs797044875
rs797044875
1.000 3 41235763 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1991 2017
dbSNP: rs864309483
rs864309483
0.851 0.080 3 123352464 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1992 2017
dbSNP: rs868985556
rs868985556
1.000 11 118478083 stop gained C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1989 2017
dbSNP: rs886041896
rs886041896
1.000 11 118494360 stop gained A/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1989 2017
dbSNP: rs1057518496
rs1057518496
1.000 2 199349006 stop gained G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 21 1989 2017
dbSNP: rs1057521083
rs1057521083
0.925 0.200 2 199348709 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 21 1989 2017