List of variants in gene combination CHRNA4, LOC100130587 reported by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_000744.7(CHRNA4):c.-182C>T	rs191789990	0.62609
NM_000744.7(CHRNA4):c.76+157T>G	rs11698563	0.47401
NM_000744.7(CHRNA4):c.-183C>T	rs183345681	0.20643
NC_000020.11:g.63361542G>A	rs12624510	0.07067
NC_000020.11:g.63361680C>T	rs67568446	0.06524
NM_000744.7(CHRNA4):c.51G>A (p.Leu17=)	rs79739740	0.05992
NM_000744.7(CHRNA4):c.76+95C>T	rs62206940	0.03853
NM_000744.7(CHRNA4):c.24G>C (p.Ala8=)	rs6089898	0.00898
NM_000744.7(CHRNA4):c.76+18G>T	rs199908363	0.00504
NM_000744.7(CHRNA4):c.9A>G (p.Leu3=)	rs80075498	0.00257
NM_000744.7(CHRNA4):c.-1C>T	rs200524076	0.00102
NM_000744.7(CHRNA4):c.42G>A (p.Pro14=)	rs565990502	0.00048
NM_000744.7(CHRNA4):c.76+14C>A	rs6090386	0.00026
NM_000744.7(CHRNA4):c.20G>C (p.Gly7Ala)	rs1025632281	0.00006
NM_000744.7(CHRNA4):c.-25C>T	rs1057518525	0.00001
NM_000744.7(CHRNA4):c.16C>T (p.Pro6Ser)	rs796052312	0.00001
NM_000744.7(CHRNA4):c.38C>G (p.Pro13Arg)	rs796052313	0.00001
NC_000020.11:g.63361453T>A	rs58134915
NC_000020.11:g.63361486A>G	rs13043186
NM_000744.7(CHRNA4):c.-28C>T	rs796052311
NM_000744.7(CHRNA4):c.-30C>A	rs6090387
NM_000744.7(CHRNA4):c.-39G>A	rs1057522008
NM_000744.7(CHRNA4):c.16C>A (p.Pro6Thr)	rs796052312
NM_000744.7(CHRNA4):c.2T>C (p.Met1Thr)	rs2068814460
NM_000744.7(CHRNA4):c.38_49dup (p.Pro13_Leu16dup)	rs1064794327
NM_000744.7(CHRNA4):c.38_52del (p.Pro13_Leu17del)	rs771936944
NM_000744.7(CHRNA4):c.41C>T (p.Pro14Leu)	rs761934698
NM_000744.7(CHRNA4):c.44T>C (p.Leu15Pro)	rs886044055
NM_000744.7(CHRNA4):c.53T>G (p.Leu18Arg)	rs796052314
NM_000744.7(CHRNA4):c.77-303G>C	rs45568238
NM_000744.7(CHRNA4):c.8T>G (p.Leu3Arg)	rs2145412488

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