List of variants in gene CYP2C19 reported as benign

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000769.1(CYP2C19):c.991A>G (p.Ile331Val)	rs3758581	0.95515
NM_000769.4(CYP2C19):c.99C>T (p.Pro33=)	rs17885098	0.92070
NM_000769.4(CYP2C19):c.1251A>C (p.Gly417=)	rs17886522	0.00780
CYP2C19*15	rs17882687	0.00626
NM_000769.1(CYP2C19):c.636G>A (p.Trp212Ter)	rs4986893	0.00149
GRCh37/hg19 10q23.33(chr10:96497751-96560546)
GRCh37/hg19 10q23.33(chr10:96528208-96541982)x1
GRCh37/hg19 10q23.33(chr10:96541982-96602398)x0
GRCh37/hg19 10q23.33(chr10:96541982-96647117)x0
NM_000769.4(CYP2C19):c.1059C>T (p.His353=)

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