Variant call file of rare variants of albinism and pigmentation genes with ≤1% frequency in gnomAD [39] seen in 45 AHM patients from the BNMS.
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资源简介：
The genes reported in this study include TYR, OCA2, TYRP1, SLC45A2, SLC24A5, LRMDA, KITLG, POMC, SLC24A4, TPCN2. (VCF)
创建时间：
2020-09-23
