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: rs1559061954
rs1559061954
1.000 0.160 2 189006937 missense variant G/T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 5 1993 2015
dbSNP: rs587779431
rs587779431
1.000 0.160 2 189008108 missense variant G/A;T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.800 1.000 5 1989 2017
dbSNP: rs587779563
rs587779563
1.000 0.160 2 189006444 missense variant G/A snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 5 1993 2015
dbSNP: rs587779588
rs587779588
1.000 0.160 2 188992194 missense variant G/A;T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.800 1.000 5 1989 2017
dbSNP: rs587779654
rs587779654
1.000 0.160 2 189004303 missense variant G/A;T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 5 1993 2015
dbSNP: rs587779688
rs587779688
1.000 0.160 2 188988648 splice region variant G/A snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 5 1993 2015
dbSNP: rs587779704
rs587779704
1.000 0.160 2 189006354 missense variant G/A;T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.800 1.000 5 1989 2017
dbSNP: rs878853651
rs878853651
1.000 0.160 2 189004276 missense variant G/A snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 5 1993 2015
dbSNP: rs397509370
rs397509370
1.000 0.160 2 188994595 splice donor variant G/A;T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 4 1990 2016
dbSNP: rs1559054653
rs1559054653
1.000 0.160 2 188990335 missense variant G/C snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 3 2014 2019
dbSNP: rs587779625
rs587779625
1.000 0.160 2 188990114 missense variant G/A snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 3 2004 2014
dbSNP: rs111929073
rs111929073
1.000 0.160 2 188999471 missense variant G/A;C;T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 2 2006 2014
dbSNP: rs587779671
rs587779671
1.000 0.160 2 188988139 splice region variant G/A;T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 2 2014 2015
dbSNP: rs112532745
rs112532745
1.000 0.160 2 189010366 splice donor variant G/T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2014 2014
dbSNP: rs1553507863
rs1553507863
1.000 0.160 2 188994061 frameshift variant T/- del
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2017 2017
dbSNP: rs1559052551
rs1559052551
1.000 0.160 2 188984759 splice acceptor variant G/C snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2014 2014
dbSNP: rs1559058970
rs1559058970
1.000 0.160 2 188999896 splice donor variant G/A snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2014 2014
dbSNP: rs1559059873
rs1559059873
1.000 0.160 2 189002295 splice acceptor variant CAGGGTG/- del
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2014 2014
dbSNP: rs1559060412
rs1559060412
1.000 0.160 2 189003426 stop gained C/T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2012 2012
dbSNP: rs1559061674
rs1559061674
1.000 0.160 2 189006335 splice acceptor variant TTGTTCACAGG/GT delins
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2014 2014
dbSNP: rs1559063681
rs1559063681
1.000 0.160 2 189010646 splice acceptor variant A/G snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2014 2014
dbSNP: rs587779495
rs587779495
1.000 0.160 2 189008054 missense variant G/A snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2014 2014
dbSNP: rs587779673
rs587779673
1.000 0.160 2 188992888 missense variant G/A snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2014 2014
dbSNP: rs587779702
rs587779702
1.000 0.160 2 188996124 splice region variant G/- delins
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.700 1.000 1 2014 2014
dbSNP: rs587779709
rs587779709
1.000 0.160 2 189006947 missense variant G/T snv
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV
0.800 1.000 1 1989 2017