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: rs5030869
rs5030869
0.882 0.120 X 154532990 missense variant C/A;T snv 5.5E-06; 1.9E-04 6.6E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 5 1981 2008
dbSNP: rs748318386
rs748318386
AUH
1.000 9 91220824 missense variant G/A;T snv 4.4E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 4 2003 2010
dbSNP: rs80359388
rs80359388
0.882 0.200 13 32337899 frameshift variant TT/-;T delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 10 1998 2011
dbSNP: rs80359541
rs80359541
0.882 0.200 13 32340183 frameshift variant C/- del 8.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 10 1998 2011
dbSNP: rs80359775
rs80359775
0.882 0.200 13 32398210 frameshift variant TATG/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 10 1998 2011
dbSNP: rs606231193
rs606231193
0.925 0.080 X 48902391 frameshift variant AGAG/-;AG;AGAGAG delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 1962 2011
dbSNP: rs797044915
rs797044915
1.000 6 33176015 splice donor variant C/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 17 1975 2012
dbSNP: rs267606653
rs267606653
0.925 11 44267607 stop gained G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 2000 2012
dbSNP: rs764358419
rs764358419
1.000 16 89649495 splice region variant G/A;T snv 1.6E-05; 1.2E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2001 2012
dbSNP: rs1331331095
rs1331331095
0.925 0.080 11 71435394 missense variant A/C;T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 16 1994 2013