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#619947 - WAARDENBURG SYNDROME, TYPE 2F; WS2F
Cytogenetic locations: 35543077
Gene summaries Genetic tests Medical literature
#616697 - DEAFNESS, AUTOSOMAL DOMINANT 69; DFNA69
Cytogenetic locations: 26522471
#611664 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 7; SHEP7
Cytogenetic locations: 17952075
*184745 - KIT LIGAND; KITLG
#145250 - HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE; FPHH
Cytogenetic locations: 15040480
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