List of variants reported as pathogenic for familial progressive hyperpigmentation

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000899.5(KITLG):c.100A>C (p.Thr34Pro)	rs730882157
NM_000899.5(KITLG):c.107A>G (p.Asn36Ser)	rs121918653
NM_000899.5(KITLG):c.108T>G (p.Asn36Lys)
NM_000899.5(KITLG):c.98T>C (p.Val33Ala)	rs730882156

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