List of variants in gene TMCO1 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
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: 10

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HGVS	dbSNP	gnomAD frequency
NM_019026.6(TMCO1):c.208+286A>G	rs61800455	0.00769
NM_019026.6(TMCO1):c.148+136T>C	rs77313837	0.00662
NM_019026.6(TMCO1):c.468+129T>C	rs149249499	0.00569
NM_019026.6(TMCO1):c.256-12G>A	rs145104339	0.00560
NM_019026.6(TMCO1):c.-66T>C	rs62622803	0.00372
NM_019026.6(TMCO1):c.256-145_256-144dup	rs151112011	0.00365
NM_019026.6(TMCO1):c.323+36A>G	rs150384701	0.00348
NM_019026.6(TMCO1):c.255+261del	rs111302957
NM_019026.6(TMCO1):c.256-103dup	rs773982057
NM_019026.6(TMCO1):c.256-187G>T	rs542510438

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