List of variants in gene RPGRIP1 reported as benign for Cone-rod dystrophy 13

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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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.1152-65G>A	rs3748357	0.34499
NM_020366.4(RPGRIP1):c.3097G>C (p.Glu1033Gln)	rs3748361	0.25511
NM_020366.4(RPGRIP1):c.1797G>A (p.Pro599=)	rs9322965	0.22187
NM_020366.4(RPGRIP1):c.1639G>T (p.Ala547Ser)	rs10151259	0.21790
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	0.05758
NM_020366.4(RPGRIP1):c.*10T>C	rs80191010	0.01626
NM_020366.4(RPGRIP1):c.3546C>T (p.Asp1182=)	rs34116882	0.01609
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.2292G>A (p.Ala764=)	rs35207255	0.00650
NM_020366.4(RPGRIP1):c.450C>G (p.Leu150=)	rs144585562	0.00130

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