Variants in gene ENG with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_001114753.3(ENG):c.392C>T (p.Pro131Leu)	rs139398993	0.00077
NM_001114753.3(ENG):c.219+22C>T	rs370257876	0.00073
NM_001114753.3(ENG):c.687C>T (p.Ala229=)	rs376919650	0.00042
NM_001114753.3(ENG):c.640G>A (p.Gly214Ser)	rs150932144	0.00034
NM_001114753.3(ENG):c.-63C>T	rs886063476	0.00028
NM_001114753.3(ENG):c.7C>T (p.Arg3Cys)	rs139334561	0.00024
NM_001114753.3(ENG):c.322C>T (p.His108Tyr)	rs756897517	0.00015
NM_001114753.3(ENG):c.1762G>A (p.Val588Ile)	rs201768056	0.00007
NM_001114753.3(ENG):c.805A>G (p.Met269Val)	rs1323617205	0.00002
NM_001114753.3(ENG):c.442G>C (p.Glu148Gln)	rs770290260	0.00001
NM_001114753.3(ENG):c.680A>G (p.His227Arg)	rs377548944	0.00001
NM_001114753.3(ENG):c.943G>A (p.Val315Met)	rs763508329	0.00001
NM_001114753.3(ENG):c.-115G>C	rs546892762

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