List of variants in gene AHI1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001134831.2(AHI1):c.396_397dup	rs397885237	0.11907
NM_001134831.2(AHI1):c.2798A>G (p.Tyr933Cys)	rs41288013	0.00466
NM_001134831.2(AHI1):c.2972G>A (p.Arg991His)	rs35851478	0.00429
NM_001134831.2(AHI1):c.2505G>A (p.Arg835=)	rs41288017	0.00383
NM_001134831.2(AHI1):c.1791C>T (p.Ile597=)	rs150425546	0.00307
NM_001134831.2(AHI1):c.724C>T (p.Pro242Ser)	rs143522987	0.00307
NM_001134831.2(AHI1):c.3039G>A (p.Gln1013=)	rs142381345	0.00194
NM_001134831.2(AHI1):c.3164C>T (p.Thr1055Met)	rs73559947	0.00159
NM_001134831.2(AHI1):c.3257A>G (p.Glu1086Gly)	rs148000791	0.00115
NM_001134831.2(AHI1):c.3342A>G (p.Glu1114=)	rs199708272	0.00041
NM_001134831.2(AHI1):c.3418C>T (p.Pro1140Ser)	rs201148693	0.00031
NM_001134831.2(AHI1):c.2589G>A (p.Glu863=)	rs147279669	0.00029
NM_001134831.2(AHI1):c.82C>T (p.Arg28Cys)	rs199612496	0.00011
NM_001134831.2(AHI1):c.2945G>T (p.Arg982Met)	rs370400336	0.00009
NM_001134831.2(AHI1):c.653A>G (p.Tyr218Cys)	rs183936286	0.00009
NM_001134831.2(AHI1):c.2567C>G (p.Thr856Ser)	rs199736888

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