List of variants in gene RPGRIP1 reported as benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_020366.4(RPGRIP1):c.574A>G (p.Lys192Glu)	rs6571751	0.48811
NM_020366.4(RPGRIP1):c.3097G>C (p.Glu1033Gln)	rs3748361	0.25511
NM_020366.4(RPGRIP1):c.1797G>A (p.Pro599=)	rs9322965	0.22045
NM_020366.4(RPGRIP1):c.1639G>T (p.Ala547Ser)	rs10151259	0.21481
NM_020366.4(RPGRIP1):c.2215+7G>A	rs7157052	0.19970
NM_020366.4(RPGRIP1):c.525A>G (p.Pro175=)	rs17792599	0.16008
NM_020366.4(RPGRIP1):c.287C>A (p.Pro96Gln)	rs1040904	0.05695
NM_020366.4(RPGRIP1):c.3340-15C>T	rs28664100	0.05325
NM_020366.4(RPGRIP1):c.3341A>G (p.Asp1114Gly)	rs17103671	0.02500
NM_020366.4(RPGRIP1):c.3719G>A (p.Gly1240Glu)	rs34725281	0.02281
NM_020366.4(RPGRIP1):c.3546C>T (p.Asp1182=)	rs34116882	0.01609
NM_020366.4(RPGRIP1):c.*10T>C	rs80191010	0.01514
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.1767G>T (p.Gln589His)	rs34067949	0.00345
NM_020366.4(RPGRIP1):c.2284C>T (p.Leu762=)	rs145896974	0.00240
NM_020366.4(RPGRIP1):c.450C>G (p.Leu150=)	rs144585562	0.00167
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	0.00005
NM_020366.4(RPGRIP1):c.907-25AAT[3]	rs398099213

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