ClinVar Miner

List of variants in gene combination MYOT, PKD2L2-DT reported by Fulgent Genetics, Fulgent Genetics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006790.3(MYOT):c.1190+12A>G	rs183456886	0.00055
NM_006790.3(MYOT):c.1286C>G (p.Ala429Gly)	rs144731446	0.00012
NM_006790.3(MYOT):c.1401T>A (p.Asn467Lys)	rs145427063
NM_006790.3(MYOT):c.179C>G (p.Ser60Cys)	rs121908458

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