ClinVar Miner

List of variants in gene combination LOC108281180, NF1 reported by UAB Medical Genomics Laboratory, UAB Medicine

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_000267.3(NF1):c.288+230_480-1812delins323
NM_000267.3(NF1):c.289-1237_586+3325del
NM_000267.3(NF1):c.289-950_586+3043del
NM_000267.3(NF1):c.289-956_586+4999del

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