Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs180177035
rs180177035
0.752 0.280 7 140801502 missense variant T/C snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 10 1968 2013
dbSNP: rs180177040
rs180177040
0.790 0.360 7 140754187 missense variant T/C;G snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 1968 2013
dbSNP: rs180177041
rs180177041
0.851 0.240 7 140777006 missense variant C/G snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 1968 2013
dbSNP: rs180177042
rs180177042
0.807 0.280 7 140749365 missense variant A/C;T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 1968 2013
dbSNP: rs387906660
rs387906660
0.790 0.280 7 140801550 missense variant G/A;C;T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 1968 2013
dbSNP: rs397507469
rs397507469
0.882 0.200 7 140801503 missense variant G/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 1968 2013
dbSNP: rs397516893
rs397516893
0.925 0.160 7 140778048 missense variant A/C snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 1968 2013
dbSNP: rs869025340
rs869025340
0.925 0.160 7 140777032 missense variant A/C;G;T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 1968 2013