ClinVar Miner

List of variants in gene ADGRB2 reported as benign for not provided

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Gene type:
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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_001364857.2(ADGRB2):c.4551A>G (p.Ala1517=) rs1127100 0.67441
NM_001364857.2(ADGRB2):c.1418-13A>C rs2297600 0.33542
NM_001364857.2(ADGRB2):c.525C>T (p.Pro175=) rs4949223 0.11031
NM_001364857.2(ADGRB2):c.2168-18A>C rs12749187 0.07383
NM_001364857.2(ADGRB2):c.4113G>C (p.Glu1371Asp) rs61744431 0.02806
NM_001364857.2(ADGRB2):c.2619T>C (p.His873=) rs61741785 0.02746
NM_001364857.2(ADGRB2):c.3892C>T (p.Leu1298=) rs10914473 0.02437
NM_001364857.2(ADGRB2):c.3663G>A (p.Arg1221=) rs61742965 0.02372
NM_001364857.2(ADGRB2):c.4197G>A (p.Leu1399=) rs61744251 0.02223
NM_001364857.2(ADGRB2):c.4508C>T (p.Thr1503Met) rs77499146 0.00971
NM_001364857.2(ADGRB2):c.4730C>T (p.Pro1577Leu) rs74431877 0.00796
NM_001364857.2(ADGRB2):c.4516-17G>A rs141155138 0.00731
NM_001364857.2(ADGRB2):c.4594C>T (p.Arg1532Cys) rs41263977 0.00721
NM_001364857.2(ADGRB2):c.3222C>T (p.Gly1074=) rs113351457 0.00427
NM_001364857.2(ADGRB2):c.3267+11G>A rs113133865 0.00427
NM_001364857.2(ADGRB2):c.4716G>A (p.Glu1572=) rs149701008 0.00424
NM_001364857.2(ADGRB2):c.2558C>T (p.Pro853Leu) rs112847200 0.00423
NM_001364857.2(ADGRB2):c.4515+10C>T rs188544949 0.00414
NM_001364857.2(ADGRB2):c.3702C>T (p.Asn1234=) rs140777869 0.00363
NM_001364857.2(ADGRB2):c.4554C>G (p.Ala1518=) rs146421594 0.00275
NM_001364857.2(ADGRB2):c.3353+12G>A rs2271930 0.00175
NM_001364857.2(ADGRB2):c.4275G>A (p.Pro1425=) rs41311144 0.00135
NM_001364857.2(ADGRB2):c.2224A>T (p.Met742Leu) rs148929083 0.00078
NM_001364857.2(ADGRB2):c.2508C>T (p.Ala836=) rs200832626 0.00038
NM_001364857.2(ADGRB2):c.3760+11C>T rs146433313 0.00038
NM_001364857.2(ADGRB2):c.1839G>A (p.Glu613=)
NM_001364857.2(ADGRB2):c.2091C>T (p.Val697=)
NM_001364857.2(ADGRB2):c.2602-8C>T
NM_001364857.2(ADGRB2):c.2646-14C>T
NM_001364857.2(ADGRB2):c.2877-12G>A
NM_001364857.2(ADGRB2):c.3201-8C>G rs201681314
NM_001364857.2(ADGRB2):c.3351C>T (p.Ala1117=)
NM_001364857.2(ADGRB2):c.3353+11G>C rs186740027
NM_001364857.2(ADGRB2):c.3353+12del
NM_001364857.2(ADGRB2):c.3353+12dup rs759961385
NM_001364857.2(ADGRB2):c.342C>A (p.Pro114=) rs60306848
NM_001364857.2(ADGRB2):c.363G>A (p.Ala121=)
NM_001364857.2(ADGRB2):c.4134G>C (p.Pro1378=) rs909001
NM_001364857.2(ADGRB2):c.414G>T (p.Gly138=)
NM_001364857.2(ADGRB2):c.4416+11TG[3]
NM_001364857.2(ADGRB2):c.932C>T (p.Ala311Val)
NM_001364857.2(ADGRB2):c.972G>A (p.Thr324=)

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