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

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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.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.930+3A>G	rs150107283	0.00419
NM_020366.4(RPGRIP1):c.218+13C>G	rs200225522	0.00279
NM_020366.4(RPGRIP1):c.2376G>A (p.Ser792=)	rs185667326	0.00183
NM_020366.4(RPGRIP1):c.2599C>T (p.Arg867Trp)	rs186803989	0.00181
NM_020366.4(RPGRIP1):c.1753C>T (p.Pro585Ser)	rs147586703	0.00155
NM_020366.4(RPGRIP1):c.1920C>T (p.Ala640=)	rs368434311	0.00029
NM_020366.4(RPGRIP1):c.2725A>G (p.Thr909Ala)	rs759254680	0.00010
NM_020366.4(RPGRIP1):c.1965C>T (p.Thr655=)	rs781676562	0.00001
NM_020366.4(RPGRIP1):c.708G>A (p.Glu236=)	rs770273789	0.00001

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