"PreventionGenetics, part of Exact Sciences"[submitter] AND "ARIH1"[ge - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1556148	NM_005744.5(ARIH1):c.75GGA[3] (p.Glu28del)	ARIH1 (E28del)	Microsatellite (inframe_deletion)	not provided +2 more	GBenign/Likely benign
Select item 1349171	NM_005744.5(ARIH1):c.237CGG[9] (p.Gly89_Gly90dup)	ARIH1	Microsatellite (inframe_insertion)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 402394	NM_005744.5(ARIH1):c.237CGG[8] (p.Gly90dup)	ARIH1	Microsatellite (inframe_insertion)	ARIH1-related disorder +2 more	GBenign
Select item 1424076	NM_005744.5(ARIH1):c.237CGG[4] (p.Gly88_Gly90del)	ARIH1	Microsatellite (inframe_deletion)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3037705	NM_005744.5(ARIH1):c.255C>T (p.Gly85=)	ARIH1	Single nucleotide variant (synonymous variant)	ARIH1-related disorder	GLikely benign
Select item 1639449	NM_005744.5(ARIH1):c.633C>T (p.Cys211=)	ARIH1	Single nucleotide variant (synonymous variant)	ARIH1-related disorder +2 more	GBenign
Select item 1655231	NM_005744.5(ARIH1):c.681+6G>A	ARIH1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2049924	NM_005744.5(ARIH1):c.1215+9A>G	ARIH1	Single nucleotide variant (intron variant)	ARIH1-related disorder +1 more	GBenign/Likely benign
Select item 1544882	NM_005744.5(ARIH1):c.1302A>G (p.Leu434=)	ARIH1	Single nucleotide variant (synonymous variant)	ARIH1-related disorder +1 more	GBenign/Likely benign