List of variants in gene GANAB reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_198334.3(GANAB):c.548C>T (p.Ala183Val)	rs921091711	0.00008
NM_198334.3(GANAB):c.926G>A (p.Arg309His)	rs144118755	0.00008
NM_198334.3(GANAB):c.253G>A (p.Val85Met)	rs1033126561	0.00006
NM_198334.3(GANAB):c.381-10T>C	rs371678104	0.00006
NM_198334.3(GANAB):c.2334C>A (p.Asp778Glu)	rs937056702	0.00005
NM_198334.3(GANAB):c.2093G>A (p.Arg698Gln)	rs765000469	0.00004
NM_198334.3(GANAB):c.323C>T (p.Pro108Leu)	rs200232092	0.00002
NM_198334.3(GANAB):c.560+469C>T	rs777394229	0.00002
NM_198334.3(GANAB):c.2177T>C (p.Met726Thr)	rs772357517	0.00001
NM_198334.3(GANAB):c.415G>A (p.Glu139Lys)	rs1033886387	0.00001
NM_198334.3(GANAB):c.1142G>C (p.Ser381Thr)	rs1043983959
NM_198334.3(GANAB):c.2021G>A (p.Arg674Gln)	rs2134469442

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