ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.4360G>C (p.Asp1454His)	rs1057518938
NM_017668.3(NDE1):c.*388del	rs543763112

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