List of variants in gene TNXB reported as likely benign for vesicoureteral reflux

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001365276.2(TNXB):c.113G>A (p.Arg38Gln)	rs149502087	0.00876
NM_001365276.2(TNXB):c.4484C>T (p.Thr1495Ile)	rs6910390	0.00842
NM_001365276.2(TNXB):c.2385A>G (p.Thr795=)	rs185461070	0.00300
NM_001365276.2(TNXB):c.2811C>A (p.Thr937=)	rs140665128	0.00166
NM_001365276.2(TNXB):c.7802C>T (p.Pro2601Leu)	rs575866552	0.00053
NM_001365276.2(TNXB):c.4209C>T (p.Thr1403=)	rs148934769	0.00047
NM_001365276.2(TNXB):c.9762C>T (p.Pro3254=)	rs190855421	0.00047
NM_001365276.2(TNXB):c.8468-1G>A	rs200718357	0.00039
NM_001365276.2(TNXB):c.7413T>C (p.Pro2471=)	rs375764263	0.00016
NM_001365276.2(TNXB):c.7417C>T (p.Arg2473Cys)	rs373029180	0.00014
NM_001365276.2(TNXB):c.9637A>G (p.Arg3213Gly)	rs377386505	0.00013
NM_001365276.2(TNXB):c.6303A>G (p.Leu2101=)	rs761030884	0.00012
NM_001365276.2(TNXB):c.5442C>G (p.Asp1814Glu)	rs181025235

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