List of variants in gene SETD5 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001080517.3(SETD5):c.3944C>T (p.Thr1315Met)	rs202179816	0.00039
NM_001080517.3(SETD5):c.2006G>C (p.Gly669Ala)	rs199595728	0.00033
NM_001080517.3(SETD5):c.1525-5T>C	rs532565367	0.00007
NM_001080517.3(SETD5):c.245C>T (p.Pro82Leu)	rs746405582	0.00001
NM_001080517.3(SETD5):c.2922C>T (p.Asp974=)	rs1049067352	0.00001
NM_001080517.3(SETD5):c.330-3T>C	rs775547620	0.00001
NM_001080517.3(SETD5):c.3824G>A (p.Arg1275Gln)	rs1283153458	0.00001
NM_001080517.3(SETD5):c.1441-10T>C	rs1553623867
NM_001080517.3(SETD5):c.330-6C>T	rs1448139711
NM_001080517.3(SETD5):c.3862G>A (p.Gly1288Ser)	rs755607090

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