List of variants in gene CHRNB2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000748.3(CHRNB2):c.1233G>A (p.Ala411=)	rs55857552	0.00330
NM_000748.3(CHRNB2):c.1235G>A (p.Gly412Asp)	rs112585933	0.00133
NM_000748.3(CHRNB2):c.1485C>T (p.Asp495=)	rs144813907	0.00088
NM_000748.3(CHRNB2):c.1482A>G (p.Ser494=)	rs8192486	0.00058
NM_000748.3(CHRNB2):c.1128C>T (p.Leu376=)	rs113116986	0.00024
NM_000748.3(CHRNB2):c.109C>T (p.Leu37=)	rs71651693	0.00011
NM_000748.3(CHRNB2):c.825G>A (p.Ala275=)	rs140739605	0.00007
NM_000748.3(CHRNB2):c.297T>C (p.Phe99=)	rs777276160	0.00005
NM_000748.3(CHRNB2):c.201C>T (p.Leu67=)	rs773706734	0.00004
NM_000748.3(CHRNB2):c.1257G>T (p.Pro419=)	rs199743038	0.00001
NM_000748.3(CHRNB2):c.1308C>T (p.Asp436=)	rs1057524421	0.00001
NM_000748.3(CHRNB2):c.1378C>G (p.Arg460Gly)	rs202079239
NM_000748.3(CHRNB2):c.174A>G (p.Val58=)

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