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: rs1189463428
rs1189463428
1.000 0.040 2 222297003 missense variant C/T snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 1.000 19 1992 2012
dbSNP: rs1020175890
rs1020175890
1.000 0.040 2 222221362 missense variant C/T snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 1.000 1 2014 2014
dbSNP: rs1553575159
rs1553575159
1.000 0.040 2 222232080 stop gained G/A snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 1.000 1 2018 2018
dbSNP: rs1553575179
rs1553575179
1.000 0.040 2 222232131 frameshift variant AATGTCAGGGTAA/- delins
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 1.000 1 2018 2018
dbSNP: rs1553592766
rs1553592766
1.000 0.040 2 222294289 frameshift variant C/- del
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 1.000 1 2018 2018
dbSNP: rs1553593965
rs1553593965
1.000 0.040 2 222297139 inframe deletion GTTGGGCAGCGG/- delins
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 1.000 1 2018 2018
dbSNP: rs773327091
rs773327091
1.000 0.040 2 222297175 missense variant C/A;G snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 1.000 1 2018 2018
dbSNP: rs104893651
rs104893651
0.925 0.040 2 222297048 missense variant G/A snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1356246522
rs1356246522
1.000 0.040 2 222297089 stop gained G/A;T snv 4.0E-06
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1379006499
rs1379006499
1.000 0.040 2 222294310 intron variant G/A;T snv 7.0E-06
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs147111779
rs147111779
1.000 0.040 2 222202134 stop gained G/A;C snv 2.8E-05 2.1E-05
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553568831
rs1553568831
1.000 0.040 2 222201988 frameshift variant -/TGTA delins
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553572740
rs1553572740
1.000 0.040 2 222220292 stop gained G/A snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553572946
rs1553572946
1.000 0.040 2 222221259 frameshift variant C/- del
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553572967
rs1553572967
0.925 0.040 2 222221300 frameshift variant -/C delins
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553575157
rs1553575157
1.000 0.040 2 222232079 missense variant T/G snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553575191
rs1553575191
1.000 0.040 2 222232178 missense variant A/G snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553592703
rs1553592703
1.000 0.040 2 222294222 frameshift variant -/AG ins
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553592713
rs1553592713
1.000 0.040 2 222294228 frameshift variant -/T delins
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553592757
rs1553592757
1.000 0.040 2 222294269 frameshift variant ATT/TA delins
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553593874
rs1553593874
1.000 0.040 2 222297030 missense variant T/C snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553593917
rs1553593917
1.000 0.040 2 222297067 missense variant C/A snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553594009
rs1553594009
1.000 0.040 2 222297162 frameshift variant -/T delins
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1553594069
rs1553594069
1.000 0.040 2 222297215 splice acceptor variant T/C snv
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0
dbSNP: rs1559316535
rs1559316535
1.000 0.040 2 222294194 frameshift variant GT/- delins
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
0.700 0