ClinVar Miner

List of variants in gene CHRNB2 reported as likely benign by GeneDx

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Gene type:
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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_000748.2(CHRNB2):c.-296G>A rs2072658 0.01801
NM_000748.3(CHRNB2):c.65-99A>T rs8192484 0.01602
NM_000748.3(CHRNB2):c.65-221G>A rs138398618 0.01311
NM_000748.3(CHRNB2):c.1339-183C>T rs78672525 0.00780
NM_000748.3(CHRNB2):c.*231G>A rs115971480 0.00759
NM_000748.3(CHRNB2):c.64+244C>T rs116645052 0.00678
NM_000748.3(CHRNB2):c.64+185G>A rs374065637 0.00503
NM_000748.3(CHRNB2):c.150C>T (p.Thr50=) rs149921259 0.00039
NM_000748.3(CHRNB2):c.1234G>A (p.Gly412Ser) rs774449832 0.00016
NM_000748.3(CHRNB2):c.109C>T (p.Leu37=) rs71651693 0.00011
NM_000748.3(CHRNB2):c.1488C>T (p.His496=) rs200582284 0.00008
NM_000748.3(CHRNB2):c.825G>A (p.Ala275=) rs140739605 0.00007
NM_000748.3(CHRNB2):c.1236C>T (p.Gly412=) rs767533378 0.00005
NM_000748.3(CHRNB2):c.348T>C (p.Asp116=) rs78921047 0.00005
NM_000748.3(CHRNB2):c.122G>A (p.Arg41His) rs199999862 0.00004
NM_000748.3(CHRNB2):c.201C>T (p.Leu67=) rs773706734 0.00004
NM_000748.3(CHRNB2):c.372C>T (p.Asp124=) rs151054217 0.00004
NM_000748.3(CHRNB2):c.105T>A (p.His35Gln) rs141689121 0.00003
NM_000748.3(CHRNB2):c.316C>T (p.Arg106Trp) rs372273025 0.00003
NM_000748.3(CHRNB2):c.1035G>T (p.Ala345=) rs778458803 0.00002
NM_000748.3(CHRNB2):c.1114G>A (p.Gly372Ser) rs753731408 0.00002
NM_000748.3(CHRNB2):c.453C>T (p.Tyr151=) rs781506269 0.00002
NM_000748.3(CHRNB2):c.1087C>T (p.Leu363=) rs201040879 0.00001
NM_000748.3(CHRNB2):c.1153G>A (p.Asp385Asn) rs932622161 0.00001
NM_000748.3(CHRNB2):c.1253A>G (p.Glu418Gly) rs1475853887 0.00001
NM_000748.3(CHRNB2):c.1287C>T (p.Asp429=) rs1057524461 0.00001
NM_000748.3(CHRNB2):c.1308C>T (p.Asp436=) rs1057524421 0.00001
NM_000748.3(CHRNB2):c.1380C>T (p.Arg460=) rs373985042 0.00001
NM_000748.3(CHRNB2):c.1425C>T (p.Ile475=) rs773226966 0.00001
NM_000748.3(CHRNB2):c.255+15T>G rs374367624 0.00001
NM_000748.3(CHRNB2):c.294G>A (p.Glu98=) rs367899705 0.00001
NM_000748.3(CHRNB2):c.613A>G (p.Ile205Val) rs568750665 0.00001
NM_000748.3(CHRNB2):c.615C>T (p.Ile205=) rs202243284 0.00001
NM_000748.3(CHRNB2):c.75T>C (p.Gly25=) rs764498388 0.00001
NM_000748.3(CHRNB2):c.912C>A (p.Thr304=) rs748080172 0.00001
NM_000748.3(CHRNB2):c.*13T>C rs749294108
NM_000748.3(CHRNB2):c.1146A>C (p.Pro382=) rs201986342
NM_000748.3(CHRNB2):c.1171G>C (p.Val391Leu) rs770055798
NM_000748.3(CHRNB2):c.123C>A (p.Arg41=) rs201171352
NM_000748.3(CHRNB2):c.1242G>C (p.Gly414=) rs1553204404
NM_000748.3(CHRNB2):c.1249G>A (p.Gly417Arg) rs1057520852
NM_000748.3(CHRNB2):c.1257G>A (p.Pro419=) rs199743038
NM_000748.3(CHRNB2):c.1338+25G>A rs56146528
NM_000748.3(CHRNB2):c.702G>A (p.Pro234=) rs200050755
NM_000748.3(CHRNB2):c.777A>T (p.Pro259=) rs770431355
NM_000748.3(CHRNB2):c.841C>T (p.Leu281=) rs1553204296

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