List of variants in gene CHRNG reported by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005199.5(CHRNG):c.125G>A (p.Arg42Gln)	rs148468628	0.00262
NM_005199.5(CHRNG):c.471C>T (p.Phe157=)	rs143272752	0.00120
NM_005199.5(CHRNG):c.543G>A (p.Gln181=)	rs753990044	0.00010
NM_005199.5(CHRNG):c.256C>T (p.Arg86Cys)	rs777219451	0.00001

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