ClinVar Miner

List of variants in gene combination CHRM2, LOC349160 reported by GeneDx

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_001006630.2(CHRM2):c.-124-41383T>A rs28529003 0.64905
NM_001006630.2(CHRM2):c.-124-41317C>T rs6960707 0.63761
NM_001006630.2(CHRM2):c.*295T>A rs8191992 0.59512
NM_001006630.2(CHRM2):c.-46-306G>T rs324651 0.14789
NM_001006630.2(CHRM2):c.-70T>C rs36210736 0.04538
NM_001006630.2(CHRM2):c.-124-41185G>A rs74662321 0.02302
NM_001006630.2(CHRM2):c.-124-41158G>T rs116292369 0.02175
NM_001006630.2(CHRM2):c.-46-328T>C rs17168883 0.01594
NM_001006630.2(CHRM2):c.-92T>C rs78848012 0.01080
NM_001006630.2(CHRM2):c.1197T>C (p.Thr399=) rs34586275 0.00676
NM_001006630.2(CHRM2):c.-46-202T>C rs141936929 0.00516
NM_001006630.2(CHRM2):c.-64C>G rs77494695 0.00496
NM_001006630.2(CHRM2):c.691G>A (p.Val231Ile) rs76394680 0.00348
NM_001006630.2(CHRM2):c.-116C>T rs79607027 0.00131
NM_001006630.2(CHRM2):c.773A>G (p.Asn258Ser) rs142006633 0.00128
NM_001006630.2(CHRM2):c.1114C>G (p.Pro372Ala) rs138806839 0.00073
NM_001006630.2(CHRM2):c.1050A>G (p.Ser350=) rs60372903 0.00070
NM_001006630.2(CHRM2):c.456C>T (p.Phe152=) rs148163637 0.00064
NM_001006630.2(CHRM2):c.991A>T (p.Thr331Ser) rs146328962 0.00064
NM_001006630.2(CHRM2):c.860C>G (p.Thr287Ser) rs138193709 0.00053
NM_001006630.2(CHRM2):c.549T>C (p.Asn183=) rs141951417 0.00044
NM_001006630.2(CHRM2):c.150C>T (p.Val50=) rs144511065 0.00039
NM_001006630.2(CHRM2):c.674T>A (p.Val225Asp) rs143952141 0.00031
NM_001006630.2(CHRM2):c.757G>A (p.Asp253Asn) rs140681489 0.00030
NM_001006630.2(CHRM2):c.1059T>C (p.Asn353=) rs143722099 0.00019
NM_001006630.2(CHRM2):c.703C>A (p.Leu235Met) rs138886480 0.00014
NM_001006630.2(CHRM2):c.1251C>A (p.Ile417=) rs770736119 0.00003
NM_001006630.2(CHRM2):c.54T>C (p.Tyr18=) rs1441209174 0.00001
NM_001006630.2(CHRM2):c.*238C>G rs73447175
NM_001006630.2(CHRM2):c.-124-41403TGT[14] rs200954535
NM_001006630.2(CHRM2):c.-124-41403TGT[16] rs200954535
NM_001006630.2(CHRM2):c.-124-41403TGT[17] rs200954535
NM_001006630.2(CHRM2):c.-46-187G>C rs17168888
NM_001006630.2(CHRM2):c.-46-187G>T rs17168888
NM_001006630.2(CHRM2):c.-48T>G rs1300851768
NM_001006630.2(CHRM2):c.-49A>T rs1057524597
NM_001006630.2(CHRM2):c.1044G>A (p.Gly348=) rs1057523853
NM_001006630.2(CHRM2):c.47G>A (p.Ser16Asn) rs771580504
NM_001006630.2(CHRM2):c.67G>A (p.Val23Met) rs1057518509
NM_001006630.2(CHRM2):c.874_882del (p.Val292_Ser294del) rs1454380573

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