List of variants in gene IFT56 studied for biliary, renal, neurologic, and skeletal syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_024926.4(IFT56):c.1069+1G>A
NM_024926.4(IFT56):c.1331C>T (p.Pro444Leu)	rs2130872867
NM_024926.4(IFT56):c.4-1G>C	rs2130770516
NM_024926.4(IFT56):c.476C>T (p.Ser159Leu)
NM_024926.4(IFT56):c.788A>G (p.Asn263Ser)	rs1794039778

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