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: rs1064797102
rs1064797102
0.827 0.120 8 91071136 splice acceptor variant A/G snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs1064797103
rs1064797103
0.827 0.280 8 91078597 missense variant A/G snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs1131690789
rs1131690789
1.000 X 47181316 frameshift variant AG/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs1281877795
rs1281877795
1.000 2 55249467 frameshift variant CTTTTTTCACT/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs1553878198
rs1553878198
1.000 4 26406245 missense variant C/G snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs1555740650
rs1555740650
0.807 0.240 19 49596253 stop gained G/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs1555933969
rs1555933969
1.000 X 41216161 frameshift variant T/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs1556024875
rs1556024875
0.882 0.160 X 123634002 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs1557189252
rs1557189252
1.000 X 54465532 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs368313959
rs368313959
0.851 0.080 8 91078383 stop gained C/T snv 1.6E-04 1.0E-04
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs397517156
rs397517156
0.851 0.200 2 39012333 missense variant T/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs759317757
rs759317757
0.807 0.280 8 91078416 frameshift variant TTAAC/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs864309508
rs864309508
0.925 0.080 15 25356778 frameshift variant CA/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs886039804
rs886039804
0.882 0.120 11 61366050 missense variant A/G snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs886039807
rs886039807
0.776 0.480 16 75541466 non coding transcript exon variant A/G snv 4.2E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs1553353206
rs1553353206
1.000 1 224398525 frameshift variant CATTTAACAA/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 1 2017 2017
dbSNP: rs1553417206
rs1553417206
1.000 2 72465341 splice acceptor variant T/C snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 1 2016 2016
dbSNP: rs746480833
rs746480833
1.000 1 154569536 missense variant C/T snv 4.0E-06; 1.2E-05 2.8E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 1 2017 2017
dbSNP: rs869320713
rs869320713
0.851 0.120 10 248370 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 1 2014 2014
dbSNP: rs886041081
rs886041081
0.925 4 185144891 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 1 2016 2016
dbSNP: rs1382444181
rs1382444181
1.000 17 76733070 frameshift variant G/- delins 8.3E-06 7.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2014 2014
dbSNP: rs140583554
rs140583554
0.925 14 20452066 missense variant C/T snv 2.4E-05 7.7E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2017 2017
dbSNP: rs1426926688
rs1426926688
1.000 9 131038920 frameshift variant AGCACAG/- del 8.0E-06 1.4E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2011 2015
dbSNP: rs1462161137
rs1462161137
1.000 17 76733042 frameshift variant -/A delins 7.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2014 2014
dbSNP: rs1479675678
rs1479675678
1.000 1 62513588 stop gained G/A;C snv 7.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2006 2014