ClinVar Miner

List of variants in gene LFNG, MIR4648 studied for Spondylocostal dysostosis 3, autosomal recessive

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_001040167.2(LFNG):c.1074-16T>C	rs143421936	0.00011
NM_001040167.2(LFNG):c.1074-11T>C
NM_001040167.2(LFNG):c.1074-19C>T

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