ClinVar Miner

List of variants in gene FANCA, LOC130059837, LOC130059838 studied for Fanconi anemia complementation group A

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 16q24.3(chr16:89764114-89781847)x0
GRCh38/hg38 16q24.3(chr16:89764796-89811592)x1
NM_000135.2(FANCA):c.1007_3066del
NM_000135.4(FANCA):c.2151+328_2778+1085del

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