List of variants in gene RBP3 reported as benign for not provided

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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: 33

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HGVS	dbSNP	gnomAD frequency
NM_002900.3(RBP3):c.-13C>T	rs41284964	0.06850
NM_002900.3(RBP3):c.2095T>C (p.Leu699=)	rs17095789	0.06119
NM_002900.3(RBP3):c.2247C>T (p.Asp749=)	rs34691259	0.02589
NM_002900.3(RBP3):c.2898C>T (p.Ser966=)	rs41284960	0.01476
NM_002900.3(RBP3):c.78C>T (p.Ser26=)	rs115562835	0.00905
NM_002900.3(RBP3):c.2077G>A (p.Val693Met)	rs112888313	0.00857
NM_002900.3(RBP3):c.1037G>A (p.Arg346His)	rs111245635	0.00786
NM_002900.3(RBP3):c.3546C>T (p.His1182=)	rs74578742	0.00786
NM_002900.3(RBP3):c.1503C>T (p.Ala501=)	rs34700898	0.00743
NM_002900.3(RBP3):c.487T>C (p.Ser163Pro)	rs35686775	0.00618
NM_002900.3(RBP3):c.1809C>T (p.Gly603=)	rs34044042	0.00571
NM_002900.3(RBP3):c.2416C>T (p.Arg806Cys)	rs35238500	0.00463
NM_002900.3(RBP3):c.3381G>A (p.Gln1127=)	rs113381589	0.00409
NM_002900.3(RBP3):c.1296G>A (p.Val432=)	rs147336433	0.00318
NM_002900.3(RBP3):c.924G>A (p.Pro308=)	rs35746996	0.00317
NM_002900.3(RBP3):c.2650G>A (p.Val884Met)	rs11204213	0.00269
NM_002900.3(RBP3):c.843C>T (p.Pro281=)	rs35186791	0.00203
NM_002900.3(RBP3):c.1933C>T (p.His645Tyr)	rs138305522	0.00200
NM_002900.3(RBP3):c.2168C>T (p.Pro723Leu)	rs148247227	0.00157
NM_002900.3(RBP3):c.63C>T (p.His21=)	rs146038948	0.00125
NM_002900.3(RBP3):c.2619C>T (p.Ala873=)	rs146045906	0.00120
NM_002900.3(RBP3):c.1635C>A (p.Thr545=)	rs145042281	0.00092
NM_002900.3(RBP3):c.120C>T (p.Cys40=)	rs373417235	0.00079
NM_002900.3(RBP3):c.927C>T (p.Ala309=)	rs75452094	0.00071
NM_002900.3(RBP3):c.3055-12C>T	rs549732319	0.00025
NM_002900.3(RBP3):c.1514A>T (p.His505Leu)	rs201808774	0.00021
NM_002900.3(RBP3):c.2626G>T (p.Ala876Ser)	rs138240045	0.00019
NM_002900.3(RBP3):c.3635C>T (p.Thr1212Ile)	rs147796755	0.00015
NM_002900.3(RBP3):c.2088C>T (p.Asp696=)	rs782425076	0.00007
NM_002900.3(RBP3):c.2556C>T (p.Ala852=)	rs375422843	0.00006
NM_002900.3(RBP3):c.1044C>T (p.Pro348=)	rs547601457	0.00001
NM_002900.3(RBP3):c.490G>T (p.Ala164Ser)	rs146287986
NM_002900.3(RBP3):c.837G>A (p.Thr279=)	rs2376635

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