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: rs1057520918
rs1057520918
0.790 0.160 19 13262780 missense variant C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 46 1988 2017
dbSNP: rs1318353774
rs1318353774
1.000 19 13298827 stop gained G/A;C snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 46 1988 2017
dbSNP: rs1555756091
rs1555756091
1.000 19 13298847 frameshift variant -/A ins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 46 1988 2017
dbSNP: rs886037945
rs886037945
0.827 0.160 19 13303584 missense variant C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 46 1988 2017
dbSNP: rs1554767317
rs1554767317
1.000 9 128203604 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 38 1983 2017
dbSNP: rs1554773487
rs1554773487
1.000 9 128220205 missense variant G/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 38 1983 2017
dbSNP: rs147001633
rs147001633
0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 36 1989 2018
dbSNP: rs1064794276
rs1064794276
NF1
0.925 0.120 17 31235639 frameshift variant TTTG/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 34 1967 2017
dbSNP: rs137854562
rs137854562
NF1
0.925 0.120 17 31235623 stop gained C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 34 1967 2017
dbSNP: rs1553583712
rs1553583712
1.000 2 165354339 frameshift variant GA/- del
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 34 1991 2017