List of variants in gene PCDH19 reported by Fulgent Genetics, Fulgent Genetics

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001184880.2(PCDH19):c.1627C>T (p.Leu543=)	rs1953337	0.19198
NM_001184880.2(PCDH19):c.402C>A (p.Ile134=)	rs41300169	0.06912
NM_001184880.2(PCDH19):c.1137C>T (p.Gly379=)	rs56277715	0.01073
NM_001184880.2(PCDH19):c.81C>T (p.Tyr27=)	rs56307810	0.00942
NM_001184880.2(PCDH19):c.655C>T (p.Leu219=)	rs377627937	0.00018
NM_001184880.2(PCDH19):c.3320G>A (p.Arg1107His)	rs200021840	0.00005
NM_001184880.2(PCDH19):c.224A>G (p.Asn75Ser)	rs796052790	0.00004
NM_001184880.2(PCDH19):c.1700C>T (p.Pro567Leu)	rs201989363
NM_001184880.2(PCDH19):c.1804C>T (p.Arg602Ter)	rs1928365677

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