List of variants in gene RAI1 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_030665.4(RAI1):c.1524G>A (p.Thr508=)	rs141826168	0.00102
NM_030665.4(RAI1):c.109G>A (p.Gly37Arg)	rs201393598	0.00024
NM_030665.4(RAI1):c.5653G>A (p.Asp1885Asn)	rs147844401	0.00014
NM_030665.4(RAI1):c.1580G>A (p.Arg527His)	rs377314203	0.00011
NM_030665.4(RAI1):c.3895G>A (p.Asp1299Asn)	rs750911924	0.00006
NM_030665.4(RAI1):c.3030C>A (p.Ala1010=)	rs542714936	0.00005
NM_030665.4(RAI1):c.3143C>A (p.Ala1048Asp)	rs758990336	0.00004
NM_030665.4(RAI1):c.3884C>T (p.Pro1295Leu)	rs376809177	0.00004
NM_030665.4(RAI1):c.5204C>T (p.Pro1735Leu)	rs376429075	0.00004
NM_030665.4(RAI1):c.719C>T (p.Thr240Ile)	rs142646842	0.00004
NM_030665.4(RAI1):c.2290G>A (p.Glu764Lys)	rs764807307	0.00003
NM_030665.4(RAI1):c.2544C>T (p.Ala848=)	rs777023372	0.00003
NM_030665.4(RAI1):c.4682G>A (p.Arg1561Gln)	rs755678482	0.00003
NM_030665.4(RAI1):c.2700C>T (p.Thr900=)	rs370400740	0.00002
NM_030665.4(RAI1):c.3146C>T (p.Ser1049Leu)	rs755152385	0.00002
NM_030665.4(RAI1):c.3590G>T (p.Gly1197Val)	rs368975225	0.00002
NM_030665.4(RAI1):c.12T>C (p.Phe4=)	rs755209169	0.00001
NM_030665.4(RAI1):c.1471G>A (p.Glu491Lys)	rs527757515	0.00001
NM_030665.4(RAI1):c.1054C>T (p.Arg352Cys)	rs907728820
NM_030665.4(RAI1):c.1665C>G (p.Thr555=)	rs769515020
NM_030665.4(RAI1):c.1740G>T (p.Pro580=)	rs138768616
NM_030665.4(RAI1):c.2931C>A (p.Asn977Lys)	rs754379238
NM_030665.4(RAI1):c.3709C>G (p.Arg1237Gly)	rs1555565828
NM_030665.4(RAI1):c.5517C>T (p.Ala1839=)	rs377747563
NM_030665.4(RAI1):c.643T>C (p.Ser215Pro)	rs1555564927
NM_030665.4(RAI1):c.76C>T (p.Arg26Cys)	rs376964045
NM_030665.4(RAI1):c.836_837del (p.Gln279fs)	rs587780429

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