"GeneDx"[submitter] AND "FABP2"[gene] - ClinVar

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Search results

Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58033	GRCh38/hg38 4q22.3-28.3(chr4:96092893-136410207)x3	LOC129993082, LOC129993083 +661 more	Copy number gain	See cases	GPathogenic
Select item 1226605	NM_000134.4(FABP2):c.*252G>A	FABP2	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1236503	NM_000134.4(FABP2):c.*65A>G	FABP2	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1226479	NM_000134.4(FABP2):c.*15G>A	FABP2	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1259953	NM_000134.4(FABP2):c.357A>G (p.Val119=)	FABP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1265548	NM_000134.4(FABP2):c.241-34TAT[13]	FABP2	Microsatellite (intron variant)	not provided	GBenign
Select item 1248668	NM_000134.4(FABP2):c.241-34TAT[11]	FABP2	Microsatellite (intron variant)	not provided	GBenign
Select item 767974	NM_000134.4(FABP2):c.241-34TAT[14]	FABP2	Microsatellite (intron variant)	not provided	GBenign
Select item 1250553	NM_000134.4(FABP2):c.241-34TAT[9]	FABP2	Microsatellite (intron variant)	not provided	GBenign
Select item 1288549	NM_000134.4(FABP2):c.241-136A>G	FABP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229026	NM_000134.4(FABP2):c.240+179T>C	FABP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1269485	NM_000134.4(FABP2):c.240+166A>G	FABP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289789	NM_000134.4(FABP2):c.240+151G>A	FABP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263767	NM_000134.4(FABP2):c.240+100G>T	FABP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232917	NM_000134.4(FABP2):c.216T>C (p.Asn72=)	FABP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 16494	NM_000134.4(FABP2):c.163A>G (p.Thr55Ala)	FABP2 (T55A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1241519	NM_000134.4(FABP2):c.68-148G>A	FABP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241534	NM_000134.4(FABP2):c.68-167T>G	FABP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266765	NM_000134.4(FABP2):c.68-315G>A	FABP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288325	NM_000134.4(FABP2):c.67+262C>A	FABP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251577	NM_000134.4(FABP2):c.67+156C>T	FABP2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229473	NC_000004.12:g.119322182del	FABP2	Deletion	not provided	GBenign
Select item 1246176	NC_000004.12:g.119322197C>T	FABP2	Single nucleotide variant	not provided	GBenign
Select item 1261472	NC_000004.12:g.119322237_119322238insCTCTA	FABP2	Insertion	not provided	GBenign
Select item 1268685	NC_000004.12:g.119322356T>C	FABP2	Single nucleotide variant	not provided	GBenign
Select item 253606	GRCh37/hg19 4q26-35.2(chr4:119437495-190904301)x3	SCOC, SCRG1 +218 more	Copy number gain	See cases	GPathogenic

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Items: 26