Related gene-specific medical variations for Gene (Select 147965) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3277583	NM_174905.4(FAM98C):c.205G>T (p.Ala69Ser)	FAM98C, LOC130064348 (A69S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3059360	NM_174905.4(FAM98C):c.190G>A (p.Ala64Thr)	FAM98C, LOC130064348 (A64T)	Single nucleotide variant (missense variant)	FAM98C-related disorder	GBenign
Select item 3038918	NM_174905.4(FAM98C):c.-2T>C	FAM98C, LOC130064347	Single nucleotide variant (5 prime UTR variant)	FAM98C-related disorder	GLikely benign
Select item 2380831	NM_174905.4(FAM98C):c.184G>A (p.Ala62Thr)	FAM98C, LOC130064348 (A62T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374079	NM_174905.4(FAM98C):c.47A>G (p.Gln16Arg)	FAM98C, LOC130064347 (Q16R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2273152	NM_174905.4(FAM98C):c.25T>C (p.Trp9Arg)	FAM98C, LOC130064347 (W9R)	Single nucleotide variant (missense variant)	not specified	GLikely benign

ClinVar