List of variants in gene TRIP11 reported as uncertain significance for connective tissue disorder

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004239.4(TRIP11):c.2102A>G (p.Asn701Ser)	rs139539448	0.00217
NM_004239.4(TRIP11):c.382G>T (p.Ala128Ser)	rs141553918	0.00133
NM_004239.4(TRIP11):c.1280T>C (p.Leu427Ser)	rs34761938	0.00103
NM_004239.4(TRIP11):c.5537C>T (p.Thr1846Ile)	rs141259390	0.00050
NM_004239.4(TRIP11):c.5900A>G (p.Asn1967Ser)	rs113605039	0.00024
NM_004239.4(TRIP11):c.950A>T (p.Asp317Val)	rs140416653	0.00023
NM_004239.4(TRIP11):c.2016T>A (p.Ala672=)	rs144317897	0.00008
NM_004239.4(TRIP11):c.5368G>C (p.Gly1790Arg)	rs751740362	0.00004
NM_004239.4(TRIP11):c.975A>G (p.Ala325=)	rs143126491	0.00003
NM_004239.4(TRIP11):c.2155G>A (p.Gly719Arg)	rs759108605	0.00002
NM_004239.4(TRIP11):c.948A>C (p.Lys316Asn)	rs766465446	0.00001
NM_004239.4(TRIP11):c.5221G>A (p.Asp1741Asn)	rs2140097408

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