List of variants in gene TMEM127 reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_017849.4(TMEM127):c.136A>G (p.Thr46Ala)	rs144659242	0.00018
NM_017849.4(TMEM127):c.444T>C (p.Tyr148=)	rs768545721	0.00002
NM_017849.4(TMEM127):c.666G>A (p.Ala222=)	rs772481029	0.00001
NM_017849.4(TMEM127):c.171C>T (p.His57=)	rs1573977723
NM_017849.4(TMEM127):c.288C>T (p.Ile96=)	rs758726687

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