List of variants in gene CEP41 reported by University of Washington Center for Mendelian Genomics, University of Washington

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_018718.3(CEP41):c.616C>G (p.Pro206Ala)	rs143303575	0.00218
NM_018718.3(CEP41):c.988G>C (p.Ala330Pro)	rs368525533	0.00025
NM_018718.3(CEP41):c.107T>C (p.Met36Thr)	rs368178632	0.00011
NM_018718.3(CEP41):c.320C>G (p.Ala107Gly)	rs141025803	0.00006
NM_018718.3(CEP41):c.725G>A (p.Arg242His)	rs191246968	0.00003
NM_018718.3(CEP41):c.253G>C (p.Ala85Pro)	rs946180222
NM_018718.3(CEP41):c.602C>G (p.Ser201Cys)	rs146662384
NM_018718.3(CEP41):c.610A>G (p.Met204Val)	rs782188831

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