List of variants in gene combination LOC106780803, TNXB reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001365276.2(TNXB):c.11412T>C (p.Asp3804=)	rs2894232	0.14383
NM_001365276.2(TNXB):c.11531-36C>A	rs71565305	0.12112
NM_001365276.2(TNXB):c.11547A>G (p.Thr3849=)	rs4711283	0.05640
NM_001365276.2(TNXB):c.11264-20G>A	rs77466839	0.01622
NM_001365276.2(TNXB):c.12058+11G>A	rs562705617	0.01186
NM_001365276.2(TNXB):c.10607-19C>A	rs773540524	0.01008
NM_001365276.2(TNXB):c.12378C>T (p.Asp4126=)	rs11755562	0.00531
NM_001365276.2(TNXB):c.10677A>G (p.Leu3559=)	rs199757950	0.00382
NM_001365276.2(TNXB):c.11530+46C>T	rs2395083	0.00290
NM_001365276.2(TNXB):c.10713C>T (p.Ser3571=)	rs758424441	0.00072
NM_001365276.2(TNXB):c.10928-16C>T	rs886038647	0.00039
NM_001365276.2(TNXB):c.11530+37C>T	rs2395084	0.00031
NM_001365276.2(TNXB):c.11184G>A (p.Leu3728=)	rs886038648	0.00009
NM_001365276.2(TNXB):c.12210+43T>G	rs41316640	0.00009
NM_001365276.2(TNXB):c.12210+39dup	rs11423899	0.00007
NM_001365276.2(TNXB):c.11650+16G>A	rs886038649	0.00003
NM_001365276.2(TNXB):c.11264-48A>G	rs2856450
NM_001365276.2(TNXB):c.12156C>G (p.Arg4052=)	rs6457479

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