ClinVar Miner

List of variants in gene RPGRIP1L 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_015272.5(RPGRIP1L):c.3811_3812insT (p.Asp1271fs)	rs776673720	0.00002
NM_015272.5(RPGRIP1L):c.2891del (p.Pro964fs)	rs2544039763

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