Variants in gene AHI1 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_001134831.2(AHI1):c.3032C>G (p.Ser1011Ter)	rs777215595	0.00005
NM_001134831.2(AHI1):c.2168G>A (p.Arg723Gln)	rs121434351	0.00003
NM_001134831.2(AHI1):c.2174G>A (p.Trp725Ter)	rs587783013	0.00001
NM_001134831.2(AHI1):c.1205del (p.Pro402fs)	rs794729195
NM_001134831.2(AHI1):c.1328T>A (p.Val443Asp)	rs121434350
NM_001134831.2(AHI1):c.1799_1802del (p.Lys600fs)	rs1786504555
NM_001134831.2(AHI1):c.1861G>T (p.Gly621Ter)	rs797045223
NM_001134831.2(AHI1):c.2037-1G>C	rs1784918128
NM_001134831.2(AHI1):c.2671C>T (p.Arg891Ter)	rs1355690902
NM_001134831.2(AHI1):c.96dup (p.Leu33fs)	rs747322175

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