List of variants in gene RPGRIP1 reported by Fulgent Genetics, Fulgent Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_020366.4(RPGRIP1):c.3447C>T (p.Tyr1149=)	rs35592908	0.00689
NM_020366.4(RPGRIP1):c.1753C>T (p.Pro585Ser)	rs147586703	0.00155
NM_020366.4(RPGRIP1):c.95T>A (p.Met32Lys)	rs200510462	0.00140
NM_020366.4(RPGRIP1):c.3402_3404del (p.Met1134_Ser1135delinsIle)	rs774522001	0.00014
NM_020366.4(RPGRIP1):c.2440C>T (p.Arg814Ter)	rs759940113	0.00001
NM_020366.4(RPGRIP1):c.2554C>T (p.Arg852Ter)	rs1429786931	0.00001

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