List of variants reported as uncertain significance for Bardet-Biedl syndrome 10 by Counsyl

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_024685.4(BBS10):c.765G>A (p.Met255Ile)	rs139658279	0.00072
NM_024685.4(BBS10):c.1264C>T (p.Arg422Trp)	rs375746803	0.00003
NM_024685.4(BBS10):c.1838A>G (p.Tyr613Cys)	rs575957641	0.00002
NM_024685.4(BBS10):c.2065A>C (p.Thr689Pro)	rs759387000	0.00002
NM_024685.4(BBS10):c.1144G>T (p.Val382Phe)	rs775492103	0.00001
NM_024685.4(BBS10):c.539G>A (p.Gly180Glu)	rs1555202697	0.00001
NM_024685.4(BBS10):c.1003TCA[1] (p.Ser336del)	rs1555202655
NM_024685.4(BBS10):c.101G>C (p.Arg34Pro)	rs137852836
NM_024685.4(BBS10):c.1337_1342del (p.Phe446_Ile447del)	rs767108821
NM_024685.4(BBS10):c.1807G>A (p.Gly603Ser)	rs756523417
NM_024685.4(BBS10):c.2030G>T (p.Gly677Val)	rs1555202553
NM_024685.4(BBS10):c.2T>C (p.Met1Thr)	rs1382481529
NM_024685.4(BBS10):c.32T>G (p.Val11Gly)	rs137852838
NM_024685.4(BBS10):c.530A>G (p.Tyr177Cys)	rs1555202700

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