List of variants in gene BBS10 reported as uncertain significance for Inborn genetic diseases

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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_024685.4(BBS10):c.886G>A (p.Ala296Thr)	rs150587582	0.00041
NM_024685.4(BBS10):c.2003A>G (p.Asn668Ser)	rs142140276	0.00018
NM_024685.4(BBS10):c.1595G>A (p.Arg532Lys)	rs142297424	0.00011
NM_024685.4(BBS10):c.1882A>G (p.Met628Val)	rs760505134	0.00004
NM_024685.4(BBS10):c.1325C>T (p.Thr442Ile)	rs780966013	0.00003
NM_024685.4(BBS10):c.198-3C>T	rs779659204	0.00003
NM_024685.4(BBS10):c.1250C>A (p.Ala417Glu)	rs537219462
NM_024685.4(BBS10):c.1522A>G (p.Thr508Ala)
NM_024685.4(BBS10):c.1525C>T (p.Pro509Ser)
NM_024685.4(BBS10):c.1640C>A (p.Ala547Asp)	rs770880993
NM_024685.4(BBS10):c.187C>G (p.Pro63Ala)
NM_024685.4(BBS10):c.1896A>G (p.Ile632Met)
NM_024685.4(BBS10):c.281T>G (p.Leu94Arg)
NM_024685.4(BBS10):c.685C>A (p.Pro229Thr)
NM_024685.4(BBS10):c.851A>G (p.Gln284Arg)
NM_024685.4(BBS10):c.899_901del (p.His300del)	rs1555202668

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