List of variants in gene IFT122 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_052989.3(IFT122):c.1273C>T (p.Arg425Trp)	rs61744639	0.00451
NM_052989.3(IFT122):c.321A>G (p.Gln107=)	rs138793724	0.00299
NM_052989.3(IFT122):c.3129C>T (p.Arg1043=)	rs76881473	0.00206
NM_052989.3(IFT122):c.273-239A>G	rs1362422868	0.00001
NM_052989.3(IFT122):c.1437C>T (p.Ile479=)
NM_052989.3(IFT122):c.3501G>A (p.Val1167=)

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