List of variants in gene CHRNB2 reported as likely benign for not specified

Minimum submission review status:		Collection method:
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: 28

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HGVS	dbSNP	gnomAD frequency
NM_000748.3(CHRNB2):c.210+9A>G	rs3926124	0.10829
NM_000748.3(CHRNB2):c.1338+14G>T	rs4845378	0.07732
NM_000748.3(CHRNB2):c.1191G>C (p.Gln397His)	rs55685423	0.00688
NM_000748.3(CHRNB2):c.1235G>A (p.Gly412Asp)	rs112585933	0.00133
NM_000748.3(CHRNB2):c.1432T>C (p.Phe478Leu)	rs79137415	0.00084
NM_000748.3(CHRNB2):c.1482A>G (p.Ser494=)	rs8192486	0.00058
NM_000748.3(CHRNB2):c.150C>T (p.Thr50=)	rs149921259	0.00039
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.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.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.912C>A (p.Thr304=)	rs748080172	0.00001
NM_000748.3(CHRNB2):c.*13T>C	rs749294108
NM_000748.3(CHRNB2):c.1171G>C (p.Val391Leu)	rs770055798
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.777A>T (p.Pro259=)	rs770431355
NM_000748.3(CHRNB2):c.841C>T (p.Leu281=)	rs1553204296

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