List of variants in gene EDA reported as uncertain significance for not provided

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001399.5(EDA):c.458G>A (p.Arg153His)	rs140642493	0.00106
NM_001399.5(EDA):c.464G>A (p.Arg155His)	rs144403117	0.00026
GRCh37/hg19 Xq13.1(chrX:68961570-69095884)x1
NM_001399.5(EDA):c.-80G>T	rs2147196753
NM_001399.5(EDA):c.1035_1046del (p.Cys346_Ala349del)
NM_001399.5(EDA):c.1176G>C (p.Ter392Tyr)	rs2020256932
NM_001399.5(EDA):c.201G>T (p.Glu67Asp)	rs727505160
NM_001399.5(EDA):c.28G>A (p.Glu10Lys)	rs754851778
NM_001399.5(EDA):c.550C>T (p.Pro184Ser)
NM_001399.5(EDA):c.570_578del (p.188PGP[2])
NM_001399.5(EDA):c.707-13T>G	rs2147511678
NM_001399.5(EDA):c.741G>T (p.Gln247His)	rs886042183
NM_001399.5(EDA):c.796C>T (p.Leu266Phe)	rs2147516247
NM_001399.5(EDA):c.910T>G (p.Tyr304Asp)

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