List of variants in gene combination CHRNA4, LOC100130587 studied 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
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000744.7(CHRNA4):c.51G>A (p.Leu17=)	rs79739740	0.05992
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.76+14C>A	rs6090386	0.00026
NM_000744.7(CHRNA4):c.35T>C (p.Leu12Pro)	rs1060503516	0.00002
NM_000744.7(CHRNA4):c.-25C>T	rs1057518525	0.00001
NM_000744.7(CHRNA4):c.38C>G (p.Pro13Arg)	rs796052313	0.00001
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.38_52dup (p.Pro13_Leu17dup)	rs771936944
NM_000744.7(CHRNA4):c.53T>G (p.Leu18Arg)	rs796052314

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