UVRAG, UV radiation resistance associated, 7405

N. diseases: 336; N. variants: 5
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: rs10899133
rs10899133 		11 75820650 intron variant C/A;T snv
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs34696509
rs34696509 		11 75841535 intron variant A/-;AA delins 0.18
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1213960426
rs1213960426 		1.000 0.200 11 76140853 missense variant C/T snv
CUI: C0406709
Disease: Hay-Wells syndrome
Hay-Wells syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Stomatognathic Diseases 0.020 1.000 2 2005 2012
dbSNP: rs1458836
rs1458836 		1.000 0.040 11 75813751 non coding transcript exon variant C/T snv 0.17
CUI: C1274648
Disease: Segmental vitiligo
Segmental vitiligo 		Skin and Connective Tissue Diseases 0.010 1.000 1 2010 2010
dbSNP: rs7933235
rs7933235 		1.000 0.040 11 75829541 intron variant A/G snv 0.21
CUI: C1274648
Disease: Segmental vitiligo
Segmental vitiligo 		Skin and Connective Tissue Diseases 0.010 1.000 1 2010 2010