List of variants in gene EDA 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001399.5(EDA):c.1001G>A (p.Arg334His)	rs142948132	0.00042
NM_001399.5(EDA):c.157C>T (p.Leu53Phe)	rs974684362	0.00002
NM_001399.5(EDA):c.463C>T (p.Arg155Cys)	rs132630312	0.00002
NM_001399.5(EDA):c.467G>A (p.Arg156His)	rs132630314	0.00001
NM_001399.5(EDA):c.1093G>A (p.Val365Met)	rs2147519270
NM_001399.5(EDA):c.181T>C (p.Tyr61His)	rs132630308
NM_001399.5(EDA):c.546_581del (p.Asn185_Pro196del)	rs397516665

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