C3469521[trait identifier] AND "GenomeConnect, ClinGen"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 419042	NM_000136.3(FANCC):c.1406C>T (p.Thr469Met)	AOPEP, FANCC (T469M)	Single nucleotide variant (missense variant)	Fanconi anemia +5 more	GUncertain significance
Select item 929781	NM_000135.4(FANCA):c.3665C>T (p.Pro1222Leu)	FANCA (P1222L)	Single nucleotide variant (missense variant)	Premature ovarian failure +2 more	GConflicting classifications of pathogenicity
Select item 1339816	GRCh37/hg19 16q24.3(chr16:89874496-89888566)x1	FANCA	Copy number loss	Fanconi anemia complementation group A	Gnot provided

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