List of variants studied for reticulate pigment disorder by Fulgent Genetics, Fulgent Genetics

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001111.5(ADAR):c.298A>G (p.Arg100Gly)	rs1466731	0.99604
NM_000424.4(KRT5):c.594C>A (p.Thr198=)	rs641621	0.22738
NM_001111.5(ADAR):c.2553C>T (p.Cys851=)	rs138927668	0.00304
NM_001110.4(ADAM10):c.326-10T>C	rs111517153	0.00184
NM_001111.5(ADAR):c.1935-19G>A	rs200651742	0.00101
NM_000424.4(KRT5):c.110G>A (p.Arg37Gln)	rs61747181	0.00018
NM_001111.5(ADAR):c.222G>A (p.Arg74=)	rs150423721	0.00010
NM_001111.5(ADAR):c.2598C>G (p.Arg866=)	rs749389266	0.00004
NM_001111.5(ADAR):c.164C>T (p.Pro55Leu)	rs187076847	0.00003
NM_001111.5(ADAR):c.500C>T (p.Thr167Ile)	rs747418036	0.00002
NM_001111.5(ADAR):c.1049C>T (p.Pro350Leu)	rs763695856	0.00001
NM_001111.5(ADAR):c.1062T>G (p.His354Gln)	rs767103774	0.00001
NM_001111.5(ADAR):c.1421G>A (p.Arg474Gln)	rs759679549	0.00001
NM_001111.5(ADAR):c.487G>A (p.Gly163Arg)	rs762094056	0.00001
NM_000424.4(KRT5):c.980T>C (p.Met327Thr)	rs58072617
NM_001111.5(ADAR):c.3019G>A (p.Gly1007Arg)	rs398122822

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