ClinVar Miner

List of variants in gene RPGRIP1L reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_015272.5(RPGRIP1L):c.3432+271T>C rs4312301 0.99318
NM_015272.5(RPGRIP1L):c.1401+292G>A rs4290466 0.82612
NM_015272.5(RPGRIP1L):c.1104-82C>T rs4133017 0.80982
NM_015272.5(RPGRIP1L):c.2959-32G>A rs7203525 0.39281
NM_015272.5(RPGRIP1L):c.*55T>A rs4784319 0.37955
NM_015272.5(RPGRIP1L):c.3836-309G>A rs4784321 0.33006
NM_015272.5(RPGRIP1L):c.1401+127A>G rs7192060 0.22379
NM_015272.5(RPGRIP1L):c.1243+106A>G rs5005161 0.21303
NM_015272.5(RPGRIP1L):c.3432+67G>A rs113961478 0.19784
NM_015272.5(RPGRIP1L):c.3428C>G (p.Thr1143Ser) rs111775292 0.14328
NM_015272.5(RPGRIP1L):c.1700-181G>A rs9889127 0.10996
NM_015272.5(RPGRIP1L):c.3936C>T (p.Asp1312=) rs4784320 0.10935
NM_015272.5(RPGRIP1L):c.3073G>A (p.Gly1025Ser) rs2111119 0.10881
NM_015272.5(RPGRIP1L):c.1029+88G>A rs35526952 0.08215
NM_015272.5(RPGRIP1L):c.530-280G>A rs74018186 0.06895
NM_015272.5(RPGRIP1L):c.530-200C>T rs62048362 0.06014
NM_015272.5(RPGRIP1L):c.685G>A (p.Ala229Thr) rs61747071 0.04969
NM_015272.5(RPGRIP1L):c.530-29G>A rs74393433 0.04932
NM_015272.5(RPGRIP1L):c.1700-212G>A rs62050412 0.04846
NM_015272.5(RPGRIP1L):c.3221-217C>T rs80247559 0.04698
NM_015272.5(RPGRIP1L):c.776+221G>A rs11075982 0.04678
NM_015272.5(RPGRIP1L):c.1401+88G>A rs12598634 0.04675
NM_015272.5(RPGRIP1L):c.2152+139T>C rs12445128 0.04666
NM_015272.5(RPGRIP1L):c.2959-265A>G rs77511317 0.04666
NM_015272.5(RPGRIP1L):c.3790G>A (p.Asp1264Asn) rs3213758 0.04663
NM_015272.5(RPGRIP1L):c.1243+67G>A rs4133018 0.04660
NM_015272.5(RPGRIP1L):c.2304+91C>T rs12600091 0.04654
NM_015272.5(RPGRIP1L):c.529+64C>A rs76665976 0.04425
NM_015272.5(RPGRIP1L):c.2305-179A>G rs61488183 0.02772
NM_015272.5(RPGRIP1L):c.2231G>A (p.Arg744Gln) rs2302677 0.02738
NM_015272.5(RPGRIP1L):c.1341G>A (p.Leu447=) rs61743997 0.02188
NM_015272.5(RPGRIP1L):c.2959-15T>C rs11863101 0.01368
NM_015272.5(RPGRIP1L):c.3548C>G (p.Ala1183Gly) rs139974543 0.00854
NM_015272.5(RPGRIP1L):c.3372C>T (p.Ser1124=) rs146902870 0.00702
NM_015272.5(RPGRIP1L):c.2925A>G (p.Val975=) rs144313291 0.00524
NM_015272.5(RPGRIP1L):c.1165A>G (p.Ile389Val) rs79708859 0.00517
NM_015272.5(RPGRIP1L):c.1340T>C (p.Leu447Ser) rs138155747 0.00322
NM_015272.5(RPGRIP1L):c.3395A>G (p.Gln1132Arg) rs561414163 0.00004
NM_015272.5(RPGRIP1L):c.-8+155C>T rs62048369
NM_015272.5(RPGRIP1L):c.2304+166_2304+167del rs140498865
NM_015272.5(RPGRIP1L):c.2305-280A>G rs16952410
NM_015272.5(RPGRIP1L):c.2684-105G>T rs75586284
NM_015272.5(RPGRIP1L):c.3295-9_3295-8del rs113083177
NM_015272.5(RPGRIP1L):c.3835+185C>A rs77008584
NM_015272.5(RPGRIP1L):c.632+16del rs559978421

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