Variants in gene TMEM127 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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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.665C>T (p.Ala222Val)	rs373951977	0.00012
NM_017849.4(TMEM127):c.217G>C (p.Gly73Arg)	rs121908820	0.00004
NM_017849.4(TMEM127):c.281G>A (p.Arg94Gln)	rs746831347	0.00003
NM_017849.4(TMEM127):c.130C>T (p.Leu44=)	rs754493061	0.00001
NM_017849.4(TMEM127):c.313C>T (p.Leu105=)	rs754465684	0.00001
NM_017849.4(TMEM127):c.354G>A (p.Pro118=)	rs1392614291	0.00001
NM_017849.4(TMEM127):c.292G>A (p.Ala98Thr)	rs369144563

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