List of variants in gene combination ADAT3, SCAMP4 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_138422.4(ADAT3):c.1069G>C (p.Glu357Gln)	rs200437566	0.00035
NM_138422.4(ADAT3):c.362C>T (p.Ser121Leu)	rs1016737811	0.00005
NM_138422.4(ADAT3):c.59C>T (p.Ala20Val)	rs764240025	0.00003
NM_138422.4(ADAT3):c.440G>A (p.Arg147Gln)	rs562447196	0.00002
NM_138422.4(ADAT3):c.67C>T (p.Leu23Phe)	rs1482874328	0.00001
NM_138422.4(ADAT3):c.436_446del (p.Ala146fs)	rs2013518652
NM_138422.4(ADAT3):c.626G>A (p.Arg209Gln)	rs751313469
NM_138422.4(ADAT3):c.62C>G (p.Pro21Arg)	rs538664300
NM_138422.4(ADAT3):c.716A>C (p.His239Pro)	rs1231511320
NM_138422.4(ADAT3):c.862G>A (p.Glu288Lys)	rs1208847224

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