ClinVar Miner

List of variants in gene ANKRD45, CACYBP, CENPL, DARS2, GAS5, GPR52, KIAA0040, KLHL20, LOC105371622, LOC112577515, LOC115801455, LOC122149309, LOC122149310, LOC122149311, LOC126805920, LOC126805921, LOC126805922, LOC126805923, LOC126805924, LOC126805925, LOC126805926, LOC126805927, LOC126805928, LOC129388635, LOC129388636, LOC129388637, LOC129388638, LOC129388639, LOC129388640, LOC129931937, LOC129931938, LOC129931939, LOC129931940, LOC129931941, LOC129931942, LOC129931943, LOC129931944, LOC129931945, LOC129931946, LOC129931947, LOC129931948, LOC129931949, LOC129931950, LOC129931951, LOC129931952, LOC129931953, LOC129931954, LOC129931955, LOC129931956, LOC129931957, LOC129931958, LOC129931959, LOC129931960, LOC129931961, LOC129931962, LOC129931963, LOC129931964, LOC129931965, MRPS14, RABGAP1L, RABGAP1L-DT, RC3H1, RC3H1-DT, SERPINC1, SLC9C2, SNORA103, SNORD44, SNORD47, SNORD74, SNORD75, SNORD76, SNORD77, SNORD78, SNORD79, SNORD80, SNORD81, TEX50, TNN, ZBTB37 studied for hereditary antithrombin deficiency

Included ClinVar conditions (1):

Hereditary antithrombin deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NC_000001.11:g.173501975_175305010del

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