Related gene-specific medical variations for Gene (Select 196792) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3092399	NM_152644.3(FAM24B):c.275A>G (p.Glu92Gly)	FAM24B, FAM24B-CUZD1 (E92G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092398	NM_152644.3(FAM24B):c.264C>G (p.Cys88Trp)	FAM24B, FAM24B-CUZD1 (C88W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092397	NM_152644.3(FAM24B):c.185C>T (p.Thr62Met)	FAM24B, FAM24B-CUZD1 (T62M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2366429	NM_152644.3(FAM24B):c.48A>G (p.Ile16Met)	FAM24B, FAM24B-CUZD1 (I16M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2208366	NM_152644.3(FAM24B):c.173A>G (p.Lys58Arg)	FAM24B, FAM24B-CUZD1 (K58R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1280358	NM_152644.3(FAM24B):c.5C>T (p.Pro2Leu)	FAM24B-CUZD1, FAM24B (P2L)	Single nucleotide variant (missense variant)	not provided	GBenign

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