Variants in gene IFT122 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_052989.3(IFT122):c.3129C>T (p.Arg1043=)	rs76881473	0.00206
NM_052989.3(IFT122):c.214T>G (p.Ser72Ala)	rs144140226	0.00077
NM_052989.3(IFT122):c.1026C>T (p.Asp342=)	rs79187669	0.00075
NM_052989.3(IFT122):c.3487T>A (p.Phe1163Ile)	rs200606803	0.00057
NM_052989.3(IFT122):c.986C>T (p.Ala329Val)	rs200915373	0.00049
NM_052989.3(IFT122):c.829C>T (p.Arg277Trp)	rs61744448	0.00038
NM_052989.3(IFT122):c.1252G>A (p.Asp418Asn)	rs148626512	0.00036
NM_052989.3(IFT122):c.1553G>A (p.Arg518His)	rs138223055	0.00034
NM_052989.3(IFT122):c.2643C>T (p.Ala881=)	rs150055466	0.00032
NM_052989.3(IFT122):c.2577G>A (p.Glu859=)	rs201077232	0.00014
NM_052989.3(IFT122):c.2721G>A (p.Ala907=)	rs371570973	0.00008
NM_052989.3(IFT122):c.1758C>G (p.His586Gln)	rs141889207	0.00006
NM_052989.3(IFT122):c.228C>T (p.Ser76=)	rs772835552	0.00005
NM_052989.3(IFT122):c.876C>T (p.Gly292=)	rs768782991	0.00005
NM_052989.3(IFT122):c.132C>G (p.Thr44=)	rs371772807

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