MS4A6A[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3210770	NM_022349.4(MS4A6A):c.608C>T (p.Thr203Ile)	MS4A6A (T203I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3210769	NM_022349.4(MS4A6A):c.434C>A (p.Ala145Asp)	MS4A6A (A173D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210767	NM_022349.4(MS4A6A):c.275C>G (p.Pro92Arg)	MS4A6A (P120R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291238	NM_022349.4(MS4A6A):c.257C>T (p.Ala86Val)	MS4A6A (A114V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272674	NM_022349.4(MS4A6A):c.162G>T (p.Leu54Phe)	MS4A6A (L54F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233235	NM_022349.4(MS4A6A):c.109C>A (p.Leu37Met)	MS4A6A (L65M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3210759	NM_022349.4(MS4A6A):c.108C>A (p.Ser36Arg)	MS4A6A (S64R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259135	NM_022349.4(MS4A6A):c.37G>A (p.Val13Met)	MS4A6A (V41M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469125	NM_022349.4(MS4A6A):c.31A>G (p.Ile11Val)	MS4A6A (I39V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign