List of variants in gene DCT studied for oculocutaneous albinism

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001922.5(DCT):c.1407G>A (p.Trp469Ter)	rs764655568	0.00004
NM_001922.5(DCT):c.118T>A (p.Cys40Ser)	rs370729240	0.00003
NM_001922.5(DCT):c.100A>C (p.Ser34Arg)
NM_001922.5(DCT):c.1307_1320del (p.Phe435_Phe436insTer)	rs1882493359
NM_001922.5(DCT):c.176G>T (p.Gly59Val)	rs1885298359
NM_001922.5(DCT):c.183C>G (p.Cys61Trp)	rs1885297366
NM_001922.5(DCT):c.212G>A (p.Trp71Ter)
NM_001922.5(DCT):c.876C>A (p.Tyr292Ter)	rs201692579

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