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: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C4021945
Disease: Abnormality of globe size
Abnormality of globe size
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0426209
Disease: amniotic fluid meconium stained
amniotic fluid meconium stained
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0240543
Disease: Bulbous nose
Bulbous nose
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0024636
Disease: Malocclusion
Malocclusion
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C1837463
Disease: Narrow face
Narrow face
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C2673410
Disease: Small midface
Small midface
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C3494422
Disease: Retrognathia
Retrognathia
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0747085
Disease: Recurrent otitis media
Recurrent otitis media
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0042454
Disease: Velopharyngeal Insufficiency
Velopharyngeal Insufficiency
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C1857679
Disease: Sloping forehead
Sloping forehead
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C1837404
Disease: High, narrow palate
High, narrow palate
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0013132
Disease: Drooling
Drooling
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0025990
Disease: Micrognathism
Micrognathism
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C1839758
Disease: Narrow forehead
Narrow forehead
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C1861324
Disease: Short philtrum
Short philtrum
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C1837218
Disease: Cleft palate, isolated
Cleft palate, isolated
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C4281993
Disease: Neonatal respiratory distress
Neonatal respiratory distress
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C0271055
Disease: Rhegmatogenous retinal detachment
Rhegmatogenous retinal detachment
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C2020284
Disease: Stickler syndrome, type 1
Stickler syndrome, type 1
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C4023357
Disease: Maternal teratogenic exposure
Maternal teratogenic exposure
0.700 0
dbSNP: rs1565679039
rs1565679039
0.701 0.400 12 47983399 stop gained T/A snv
CUI: C4072903
Disease: Primary Caesarian section
Primary Caesarian section
0.700 0