List of variants in gene combination LOC129935417, TMEM237 reported as benign for Joubert syndrome and related disorders

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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_001044385.3(TMEM237):c.9T>G (p.Thr3=)	rs6736435	0.02349
NM_001044385.3(TMEM237):c.-12G>A	rs113186360	0.01229
NM_001044385.3(TMEM237):c.33G>A (p.Glu11=)	rs544767440	0.00004

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