Related gene-specific medical variations for Gene (Select 401022) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3526386	NM_024501.3(HOXD1):c.91G>A (p.Asp31Asn)	HAGLR, HOXD1 +1 more (D31N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3526385	NM_024501.3(HOXD1):c.110T>C (p.Leu37Pro)	HAGLR, HOXD1 (L37P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3526384	NM_024501.3(HOXD1):c.59T>C (p.Val20Ala)	HAGLR, HOXD1 +1 more (V20A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3526383	NM_024501.3(HOXD1):c.26C>T (p.Ser9Leu)	HAGLR, HOXD1 (S9L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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