List of variants in gene combination LOC129934333, TMEM127 reported as benign for benign neoplasm

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_017849.4(TMEM127):c.-87C>T	rs527792197	0.00319
NM_017849.4(TMEM127):c.-59C>T	rs542087360	0.00093
NM_017849.4(TMEM127):c.53C>T (p.Pro18Leu)	rs377740271	0.00036

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