List of variants in gene combination ACD, LOC130059224 reported as likely benign for hematologic disorder

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NC_000016.10:g.67660401G>A	rs142762905	0.00004
NC_000016.10:g.67660377T>G	rs773306733	0.00002
NC_000016.10:g.67660395A>G	rs753040978	0.00002
NC_000016.10:g.67660329G>T
NC_000016.10:g.67660332G>A
NC_000016.10:g.67660341A>G
NC_000016.10:g.67660344T>A	rs1567643005
NC_000016.10:g.67660347A>G
NC_000016.10:g.67660356C>T	rs974748354
NC_000016.10:g.67660377T>C
NC_000016.10:g.67660383G>A
NC_000016.10:g.67660383G>C	rs574891736
NC_000016.10:g.67660383G>T	rs574891736
NC_000016.10:g.67660389G>A	rs2052986707
NC_000016.10:g.67660392C>T	rs1295714510
NC_000016.10:g.67660410C>G
NC_000016.10:g.67660410C>T	rs554258142
NC_000016.10:g.67660413C>G	rs766076324
NC_000016.10:g.67660419T>G

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