Related gene-specific medical variations for Gene (Select 149041) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3152653	NM_172071.4(RC3H1):c.2524A>G (p.Asn842Asp)	LOC126805924, RC3H1 (N842D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2639568	NM_172071.4(RC3H1):c.2555G>A (p.Arg852Gln)	LOC126805924, RC3H1 (R852Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2600277	NM_172071.4(RC3H1):c.2714C>A (p.Pro905His)	LOC126805924, RC3H1 (P905H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473214	NM_172071.4(RC3H1):c.2695A>G (p.Met899Val)	LOC126805924, RC3H1 (M899V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299788	NM_172071.4(RC3H1):c.2716A>G (p.Thr906Ala)	LOC126805924, RC3H1 (T906A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241648	NM_172071.4(RC3H1):c.2720A>C (p.Lys907Thr)	LOC126805924, RC3H1 (K907T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233556	NM_172071.4(RC3H1):c.2527G>A (p.Val843Met)	LOC126805924, RC3H1 (V843M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar