ClinVar Miner

List of variants in gene NFIX reported by Neuberg Centre For Genomic Medicine, NCGM

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_001365902.3(NFIX):c.1456del (p.Arg486fs)	rs2018058219
NM_001365902.3(NFIX):c.383G>A (p.Arg128Gln)	rs2145192793
NM_001365902.3(NFIX):c.629T>A (p.Leu210Ter)	rs2512941523

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