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Results 1 - 4 of 4 for OCA2
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  1. Oculocutaneous albinism 
    ... known as mutations) in several genes, including TYR, OCA2, TYRP1, and SLC45A2. Variants in the TYR gene cause type 1, variants in the OCA2 gene cause type 2, variants in the TYRP1 ...
    https://medlineplus.gov/genetics/condition/oculocutaneous-albinism - Genetics
  2. Prader-Willi syndrome 
    ... Willi syndrome, the loss of a gene called OCA2 is associated with unusually fair skin and light-colored hair. The OCA2 gene is located on the segment of chromosome ...
    https://medlineplus.gov/genetics/condition/prader-willi-syndrome - Genetics
  3. Angelman syndrome 
    ... Angelman syndrome, the loss of a gene called OCA2 is associated with light-colored hair and fair skin. The OCA2 gene is located on the segment of chromosome ...
    https://medlineplus.gov/genetics/condition/angelman-syndrome - Genetics
  4. Melanoma 
    ... melanoma. ATM BAP1 BRAF CDKN2A MC1R MITF NRAS OCA2 PLA2G6 SLC45A2 TERT TP53 TYR TYRP1 Additional Information ...
    https://medlineplus.gov/genetics/condition/melanoma - Genetics