Variants in gene RPGRIP1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 16

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HGVS	dbSNP	gnomAD frequency
NM_020366.4(RPGRIP1):c.3097G>C (p.Glu1033Gln)	rs3748361	0.25511
NM_020366.4(RPGRIP1):c.1639G>T (p.Ala547Ser)	rs10151259	0.21790
NM_020366.4(RPGRIP1):c.3341A>G (p.Asp1114Gly)	rs17103671	0.02649
NM_020366.4(RPGRIP1):c.1793G>A (p.Arg598Gln)	rs74034910	0.01504
NM_020366.4(RPGRIP1):c.2417C>T (p.Thr806Ile)	rs142796310	0.01022
NM_020366.4(RPGRIP1):c.256C>T (p.Arg86Trp)	rs62646879	0.00919
NM_020366.4(RPGRIP1):c.3447C>T (p.Tyr1149=)	rs35592908	0.00689
NM_020366.4(RPGRIP1):c.930+3A>G	rs150107283	0.00419
NM_020366.4(RPGRIP1):c.1767G>T (p.Gln589His)	rs34067949	0.00344
NM_020366.4(RPGRIP1):c.2284C>T (p.Leu762=)	rs145896974	0.00240
NM_020366.4(RPGRIP1):c.95T>A (p.Met32Lys)	rs200510462	0.00140
NM_020366.4(RPGRIP1):c.542C>G (p.Ala181Gly)	rs186266220	0.00127
NM_020366.4(RPGRIP1):c.3171C>T (p.His1057=)	rs201838837	0.00053
NM_020366.4(RPGRIP1):c.2711-13G>T	rs369991630	0.00026
NM_020366.4(RPGRIP1):c.491-3T>C	rs749376395	0.00011
NM_020366.4(RPGRIP1):c.2397C>T (p.Asn799=)	rs375546482	0.00006

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