List of variants in gene combination IFT140, TMEM204 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_024600.6(TMEM204):c.396G>A (p.Pro132=)	rs776217442	0.00006
NM_024600.6(TMEM204):c.273C>T (p.Thr91=)
NM_024600.6(TMEM204):c.513G>C (p.Leu171=)

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