Variants in gene TRIP11 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004239.4(TRIP11):c.5160+59A>G	rs117502191	0.00901
NM_004239.4(TRIP11):c.2134G>A (p.Glu712Lys)	rs143524436	0.00835
NM_004239.4(TRIP11):c.4413A>C (p.Thr1471=)	rs144780536	0.00202
NM_004239.4(TRIP11):c.5056+11C>T	rs199549473	0.00170
NM_004239.4(TRIP11):c.5125G>A (p.Ala1709Thr)	rs141965887	0.00167
NM_004239.4(TRIP11):c.5010T>C (p.Ala1670=)	rs149334552	0.00103
NM_004239.4(TRIP11):c.107A>T (p.Asp36Val)	rs186074112	0.00026
NM_004239.4(TRIP11):c.754C>A (p.Arg252=)	rs186197454	0.00025
NM_004239.4(TRIP11):c.4159G>A (p.Glu1387Lys)	rs201607866	0.00004
NM_004239.4(TRIP11):c.1432G>A (p.Ala478Thr)	rs201112407	0.00001

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