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: rs869312979
rs869312979
1.000 0.160 X 24726579 intron variant A/G snv
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 0