ClinVar Miner

List of variants in gene MAP1B reported by Epi4K Consortium

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005909.5(MAP1B):c.3316C>T (p.Arg1106Ter)	rs1554055106
NM_005909.5(MAP1B):c.819del (p.Leu274fs)	rs1554054827
NM_005909.5(MAP1B):c.907C>T (p.Arg303Ter)	rs1554054831

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