ClinVar Miner

List of variants in gene FAM149B1 reported by GeneDx

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_173348.2(FAM149B1):c.234C>T (p.Gly78=)	rs775960643	0.00005
NM_173348.2(FAM149B1):c.592_598del (p.Lys198fs)
NM_173348.2(FAM149B1):c.666_669del (p.Glu223_Gly224insTer)

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