List of variants in gene CHRNA2 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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000742.4(CHRNA2):c.373A>G (p.Thr125Ala)	rs891398	0.58886
NM_000742.4(CHRNA2):c.351C>T (p.Asp117=)	rs2565061	0.17492
NM_000742.4(CHRNA2):c.65C>T (p.Thr22Ile)	rs2472553	0.16614
NM_000742.4(CHRNA2):c.1324C>T (p.Leu442=)	rs56298562	0.01760
NM_000742.4(CHRNA2):c.913C>T (p.Leu305=)	rs114294066	0.01308
NM_000742.4(CHRNA2):c.771C>T (p.Tyr257=)	rs56229264	0.01257
NM_000742.4(CHRNA2):c.1434C>A (p.Asp478Glu)	rs56344740	0.00307
NM_000742.4(CHRNA2):c.1100G>A (p.Arg367Gln)	rs149464248	0.00091
NM_000742.4(CHRNA2):c.684C>T (p.Ser228=)	rs143536618	0.00073
NM_000742.4(CHRNA2):c.1437C>T (p.His479=)	rs374849310	0.00025
NM_000742.4(CHRNA2):c.1464+20G>A	rs377015162	0.00019
NM_000742.4(CHRNA2):c.-136-3C>T	rs765846499	0.00010
NM_000742.4(CHRNA2):c.1222G>C (p.Val408Leu)	rs771994243	0.00005
NM_000742.4(CHRNA2):c.777C>T (p.Phe259=)	rs77769511	0.00004
NM_000742.4(CHRNA2):c.1575A>G (p.Leu525=)	rs1040135347	0.00003
NM_000742.4(CHRNA2):c.1059C>T (p.His353=)	rs748482434	0.00001
NM_000742.4(CHRNA2):c.1331C>G (p.Ser444Cys)	rs772465304	0.00001
NM_000742.4(CHRNA2):c.1335G>C (p.Gly445=)	rs544902151	0.00001
NM_000742.4(CHRNA2):c.1368G>A (p.Gln456=)	rs370957296	0.00001
NM_000742.4(CHRNA2):c.141G>A (p.Thr47=)	rs1057523368	0.00001
NM_000742.4(CHRNA2):c.1464+10G>T	rs749942986	0.00001
NM_000742.4(CHRNA2):c.294+20G>A	rs748420222	0.00001
NM_000742.4(CHRNA2):c.609C>T (p.Ser203=)	rs761237311	0.00001
NM_000742.4(CHRNA2):c.1113G>T (p.Leu371=)	rs1057521828
NM_000742.4(CHRNA2):c.1174C>T (p.Pro392Ser)	rs762406891
NM_000742.4(CHRNA2):c.1181G>C (p.Arg394Pro)	rs761054762
NM_000742.4(CHRNA2):c.132C>A (p.Pro44=)	rs1397983639
NM_000742.4(CHRNA2):c.1464+10G>C	rs749942986
NM_000742.4(CHRNA2):c.150G>T (p.Pro50=)	rs758848783
NM_000742.4(CHRNA2):c.339+7G>A	rs1370162616
NM_000742.4(CHRNA2):c.449+9C>G	rs368584036

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