List of variants in gene AHI1 reported as benign by Eurofins NTD LLC (GA)

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001134831.2(AHI1):c.3426+13G>A	rs6914831	0.59084
NM_001134831.2(AHI1):c.2488C>T (p.Arg830Trp)	rs13312995	0.02035
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.2972G>A (p.Arg991His)	rs35851478	0.00429
NM_001134831.2(AHI1):c.2505G>A (p.Arg835=)	rs41288017	0.00383
NM_001134831.2(AHI1):c.517G>A (p.Ala173Thr)	rs146416468	0.00348
NM_001134831.2(AHI1):c.1791C>T (p.Ile597=)	rs150425546	0.00307
NM_001134831.2(AHI1):c.3039G>A (p.Gln1013=)	rs142381345	0.00194
NM_001134831.2(AHI1):c.3257A>G (p.Glu1086Gly)	rs148000791	0.00115

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