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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
*614843 - ODONTOGENIC AMELOBLAST-ASSOCIATED PROTEIN; ODAM
Cytogenetic locations: {Leukemia
#611724 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 8; SHEP8
Cytogenetic locations: 611239
#611664 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 7; SHEP7
Cytogenetic locations: 17952075
*611409 - OCA2 MELANOSOMAL TRANSMEMBRANE PROTEIN; OCA2
Cytogenetic locations: -
*609840 - SOLUTE CARRIER FAMILY 24 (SODIUM/POTASSIUM/CALCIUM EXCHANGER), MEMBER 4; SLC24A4
Cytogenetic locations: 24621671
*609584 - L-2-HYDROXYGLUTARATE DEHYDROGENASE; L2HGDH
Cytogenetic locations: 19911013
*606933 - TYROSINASE; TYR
Cytogenetic locations: 11642278
*605837 - HECT DOMAIN AND RCC1-LIKE DOMAIN 2; HERC2
Cytogenetic locations: 20631078
#601800 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3; SHEP3
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8, INCLUDED
*184745 - KIT LIGAND; KITLG
*155555 - MELANOCORTIN 1 RECEPTOR; MC1R
Cytogenetic locations: 16q22.1
#145250 - HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE; FPHH
Cytogenetic locations: 15040480
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