List of variants in gene ANKRD26 reported as likely pathogenic for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_014915.3(ANKRD26):c.1035_1036insT (p.Lys346Ter)	rs780613456	0.00002
NM_014915.3(ANKRD26):c.-126T>C	rs1589393792	0.00001
NM_014915.3(ANKRD26):c.2392G>T (p.Glu798Ter)	rs560561829	0.00001
NM_014915.3(ANKRD26):c.-107C>T
NM_014915.3(ANKRD26):c.-116C>G	rs1589393739
NM_014915.3(ANKRD26):c.-116C>T	rs1589393739
NM_014915.3(ANKRD26):c.-118C>A	rs1589393759
NM_014915.3(ANKRD26):c.-118C>G	rs1589393759
NM_014915.3(ANKRD26):c.-118C>T	rs1589393759
NM_014915.3(ANKRD26):c.-119C>G	rs1554800065
NM_014915.3(ANKRD26):c.-127A>T	rs1589393799
NM_014915.3(ANKRD26):c.-128G>C	rs1589393809
NM_014915.3(ANKRD26):c.-128G>T	rs1589393809
NM_014915.3(ANKRD26):c.-134G>A	rs863223318
NM_014915.3(ANKRD26):c.2329_2332del (p.Leu777fs)	rs778333097
NM_014915.3(ANKRD26):c.2476G>T (p.Glu826Ter)	rs1589257502
NM_014915.3(ANKRD26):c.4995_4998del (p.Glu1666fs)	rs1564348376

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