List of variants in gene combination RIC3, TUB reported as uncertain significance for Retinal dystrophy and obesity

Minimum submission review status:		Collection method:
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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_177972.3(TUB):c.1388-10T>G	rs150402974	0.00097
NM_177972.3(TUB):c.358G>A (p.Gly120Ser)	rs146650842	0.00043
NM_177972.3(TUB):c.364G>A (p.Ala122Thr)	rs201324153	0.00021
NM_177972.3(TUB):c.1270G>A (p.Glu424Lys)	rs370188104	0.00017
NM_177972.3(TUB):c.1232T>A (p.Leu411Gln)	rs200239459	0.00006
NM_177972.3(TUB):c.451G>A (p.Val151Met)	rs767402711	0.00006
NM_177972.3(TUB):c.1498G>A (p.Asp500Asn)	rs368907491	0.00004
NM_177972.3(TUB):c.1159G>A (p.Val387Met)	rs1214536528	0.00002
NM_177972.3(TUB):c.1210C>T (p.Arg404Cys)	rs139170512	0.00002
NM_177972.3(TUB):c.1388C>T (p.Pro463Leu)	rs369604607	0.00001
NM_177972.3(TUB):c.1425G>C (p.Glu475Asp)
NM_177972.3(TUB):c.293C>T (p.Ala98Val)	rs909748733
NM_177972.3(TUB):c.722A>G (p.Glu241Gly)
NM_177972.3(TUB):c.728C>T (p.Pro243Leu)	rs1944038804
NM_177972.3(TUB):c.885+7T>C	rs776753352

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