List of variants in gene TNXB studied for See cases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001365276.2(TNXB):c.3322G>A (p.Val1108Met)	rs121912575	0.00061
NM_001365276.2(TNXB):c.9661G>A (p.Val3221Met)	rs367685759	0.00019
NM_001365276.2(TNXB):c.2730G>A (p.Ala910=)	rs564894886	0.00011
GRCh38/hg38 6p21.33(chr6:32051369-32091833)x3
NM_001365276.2(TNXB):c.10336A>C (p.Lys3446Gln)	rs2151887878
NM_001365276.2(TNXB):c.4645C>T (p.Gln1549Ter)	rs2151921014

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