List of variants in gene BBS10 reported as likely benign for not provided

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_024685.4(BBS10):c.424G>A (p.Asp142Asn)	rs142863601	0.00738
NM_024685.4(BBS10):c.1631A>G (p.Asn544Ser)	rs34737974	0.00618
NM_024685.4(BBS10):c.1669A>G (p.Ile557Val)	rs139719799	0.00167
NM_024685.4(BBS10):c.765G>A (p.Met255Ile)	rs139658279	0.00072
NM_024685.4(BBS10):c.886G>A (p.Ala296Thr)	rs150587582	0.00041
NM_024685.4(BBS10):c.1158G>A (p.Leu386=)	rs138702315
NM_024685.4(BBS10):c.132G>A (p.Glu44=)	rs1592493136

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