List of variants in gene WDPCP reported as benign for Bardet-Biedl syndrome

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_015910.7(WDPCP):c.1915+13G>A	rs992214	0.63738
NM_015910.7(WDPCP):c.1916-6C>T	rs2421862	0.14640
NM_015910.7(WDPCP):c.802G>A (p.Gly268Ser)	rs17617459	0.04486
NM_015910.7(WDPCP):c.2063A>G (p.Asn688Ser)	rs61734468	0.00905
NM_015910.7(WDPCP):c.1333G>C (p.Ala445Pro)	rs61734466	0.00572
NM_015910.7(WDPCP):c.68C>A (p.Pro23Gln)	rs141340867	0.00398
NM_015910.7(WDPCP):c.499+20A>G	rs186575824	0.00159
NM_015910.7(WDPCP):c.1315G>A (p.Val439Ile)	rs199676595	0.00052
NM_015910.7(WDPCP):c.83A>T (p.Asp28Val)	rs144703991	0.00039
NM_015910.7(WDPCP):c.480C>T (p.Ile160=)	rs768777510	0.00024
NM_015910.7(WDPCP):c.76-15T>A	rs200557033	0.00003
NM_015910.7(WDPCP):c.624_625del	rs139878372
NM_015910.7(WDPCP):c.1749-12del
NM_015910.7(WDPCP):c.385-3del	rs559429215
NM_015910.7(WDPCP):c.76-15_76-5del	rs780314107
NM_015910.7(WDPCP):c.924A>G (p.Val308=)	rs201844706

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