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: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C1851789
Disease: Poor wound healing
Poor wound healing
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0004106
Disease: Astigmatism
Astigmatism
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C1860236
Disease: Irregular hyperpigmentation
Irregular hyperpigmentation
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C1837785
Disease: Prominent superficial veins
Prominent superficial veins
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C1849265
Disease: Overgrowth
Overgrowth
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0162834
Disease: Hyperpigmentation
Hyperpigmentation
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0151526
Disease: Premature Birth
Premature Birth
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0007933
Disease: Meibomian Cyst
Meibomian Cyst
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C2673776
Disease: Vascular tortuosity
Vascular tortuosity
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0241665
Disease: Abnormal venous morphology
Abnormal venous morphology
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0151908
Disease: Dry skin
Dry skin
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C4073245
Disease: Abnormality of neck blood vessel
Abnormality of neck blood vessel
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0038505
Disease: Sturge-Weber Syndrome
Sturge-Weber Syndrome
0.880 1.000 0 2013 2019
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0241657
Disease: Abnormality of the vasculature
Abnormality of the vasculature
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0030193
Disease: Pain
Pain
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0003081
Disease: Anisometropia
Anisometropia
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C2937220
Disease: Congenital abnormality of vein
Congenital abnormality of vein
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0542514
Disease: Blue sclera
Blue sclera
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0018916
Disease: Hemangioma
Hemangioma
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0239340
Disease: Edema of lower extremity
Edema of lower extremity
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0013595
Disease: Eczema
Eczema
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C1859882
Disease: Pigmentation of the sclera
Pigmentation of the sclera
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0232462
Disease: Decrease in appetite
Decrease in appetite
0.700 0
dbSNP: rs397514698
rs397514698
0.667 0.400 9 77797577 missense variant C/T snv
CUI: C0522035
Disease: Edema of the upper extremity
Edema of the upper extremity
0.700 0