List of variants in gene AHI1 reported as benign by PreventionGenetics, part of Exact Sciences

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_001134831.2(AHI1):c.1780-14C>T	rs2757645	0.81825
NM_001134831.2(AHI1):c.3426+13G>A	rs6914831	0.59084
NM_001134831.2(AHI1):c.3485+38G>C	rs4896141	0.23072
NM_001134831.2(AHI1):c.3165+42G>C	rs7772864	0.06222
NM_001134831.2(AHI1):c.2223T>C (p.Asp741=)	rs2273761	0.02399
NM_001134831.2(AHI1):c.2488C>T (p.Arg830Trp)	rs13312995	0.02035
NM_001134831.2(AHI1):c.1780-47C>T	rs17053651	0.01944
NM_001134831.2(AHI1):c.3053A>C (p.Gln1018Pro)	rs6940875	0.01691
NM_001134831.2(AHI1):c.3015A>G (p.Ser1005=)	rs41287054	0.01682
NM_001134831.2(AHI1):c.2624-6A>G	rs41288015	0.01635
NM_001134831.2(AHI1):c.1152-11T>G	rs113317693	0.01324
NM_001134831.2(AHI1):c.804A>C (p.Ser268=)	rs35528530	0.01078
NM_001134831.2(AHI1):c.1643G>A (p.Arg548His)	rs35433555	0.01070
NM_001134831.2(AHI1):c.3579T>C (p.Thr1193=)	rs115338154	0.00537
NM_001134831.2(AHI1):c.3368C>T (p.Ser1123Phe)	rs117447608	0.00497
NM_001134831.2(AHI1):c.2798A>G (p.Tyr933Cys)	rs41288013	0.00466
NM_001134831.2(AHI1):c.2505G>A (p.Arg835=)	rs41288017	0.00383
NM_001134831.2(AHI1):c.724C>T (p.Pro242Ser)	rs143522987	0.00307
NM_001134831.2(AHI1):c.178A>G (p.Thr60Ala)	rs115502075	0.00279
NM_001134831.2(AHI1):c.3164C>T (p.Thr1055Met)	rs73559947	0.00159
NM_001134831.2(AHI1):c.2382A>G (p.Lys794=)	rs191682790	0.00030
NM_001134831.2(AHI1):c.*28G>C	rs9494209
NM_001134831.2(AHI1):c.3485+13_3485+15del	rs540849894

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