"Color Diagnostics, LLC DBA Color Health"[submitter] AND "KCNK12"[gene - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 919550	NM_022055.2(KCNK12):c.*8544G>C	KCNK12, MSH2	Single nucleotide variant (3 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 921422	NM_022055.2(KCNK12):c.*8540C>A	KCNK12, MSH2	Single nucleotide variant (3 prime UTR variant)	Hereditary cancer-predisposing syndrome	GBenign
Select item 927421	NM_022055.2(KCNK12):c.*8536C>A	KCNK12, MSH2	Single nucleotide variant (3 prime UTR variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 920227	NM_022055.2(KCNK12):c.*8535C>A	KCNK12, MSH2	Single nucleotide variant (3 prime UTR variant)	Hereditary cancer-predisposing syndrome	GBenign
Select item 135565	NC_000002.12:g.47512385C>T	KCNK12, MSH2	Single nucleotide variant (genic downstream transcript variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 926549	NM_022055.2(KCNK12):c.*8514G>A	KCNK12, MSH2	Single nucleotide variant (3 prime UTR variant)	Hereditary cancer-predisposing syndrome	GBenign
Select item 926047	NM_022055.2(KCNK12):c.*8479G>A	KCNK12, MSH2	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign
Select item 926048	NM_022055.2(KCNK12):c.*8472G>C	KCNK12, MSH2	Single nucleotide variant (3 prime UTR variant)	Hereditary cancer-predisposing syndrome	GBenign
Select item 927126	NM_022055.2(KCNK12):c.*8468C>G	KCNK12, MSH2	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GBenign