List of variants in gene AGPAT2 reported as benign for Congenital generalized lipodystrophy type 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_006412.4(AGPAT2):c.*157C>T	rs4880119	0.76858
NM_006412.4(AGPAT2):c.*442C>G	rs6951	0.75286
NM_006412.4(AGPAT2):c.661+121T>C	rs9411215	0.67675
NM_006412.4(AGPAT2):c.183-60G>C	rs2236514	0.59568
NM_006412.4(AGPAT2):c.*517C>T	rs10320	0.23704
NM_006412.4(AGPAT2):c.-67G>C	rs146341067	0.06932
NM_006412.4(AGPAT2):c.*535C>T	rs138670030	0.01906
NM_006412.4(AGPAT2):c.317-7C>T	rs74584184	0.01776
NM_006412.4(AGPAT2):c.*239G>A	rs56310643	0.01249
NM_006412.4(AGPAT2):c.702C>T (p.Ser234=)	rs116951119	0.01094
NM_006412.4(AGPAT2):c.809C>T (p.Ala270Val)	rs142417583	0.00601
NM_006412.4(AGPAT2):c.475C>T (p.Arg159Cys)	rs142993240	0.00430
NM_006412.4(AGPAT2):c.741C>T (p.Thr247=)	rs117434864	0.00024
NM_006412.4(AGPAT2):c.*79C>G	rs112657922

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