Source: ALL
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: rs13208776
rs13208776 		0.882 0.040 6 168540944 intron variant G/A;C snv
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.810 0.500 2 2010 2011
dbSNP: rs76307059
rs76307059 		6 168600208 intron variant C/A;G;T snv
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs76307059
rs76307059 		6 168600208 intron variant C/A;G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs786200927
rs786200927 		1.000 6 168441455 splice donor variant G/T snv
CUI: C3276551
Disease: DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH
DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH 		0.700 0
dbSNP: rs875989843
rs875989843 		1.000 6 168598828 stop gained T/A;C snv 4.0E-06
CUI: C3276551
Disease: DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH
DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH 		0.700 0
dbSNP: rs13208776
rs13208776 		0.882 0.040 6 168540944 intron variant G/A;C snv
CUI: C1304470
Disease: Generalized vitiligo
Generalized vitiligo 		Skin and Connective Tissue Diseases 0.010 1.000 1 2010 2010
dbSNP: rs13208776
rs13208776 		0.882 0.040 6 168540944 intron variant G/A;C snv
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		Skin and Connective Tissue Diseases 0.010 < 0.001 1 2011 2011