List of variants reported as uncertain significance for Human HOXA1 syndromes by Illumina Laboratory Services, Illumina

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Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_005522.5(HOXA1):c.210C>T (p.His70=)	rs199620262	0.00039
NM_005522.5(HOXA1):c.*980C>G	rs777986191	0.00019
NM_005522.4(HOXA1):c.-90A>G	rs981104456	0.00012
NM_005522.5(HOXA1):c.216T>C (p.His72=)	rs886062260	0.00005
NM_005522.5(HOXA1):c.*345C>T	rs557113073	0.00003
NM_005522.5(HOXA1):c.*337G>A	rs576914419	0.00001
NM_005522.5(HOXA1):c.686C>A (p.Pro229His)	rs759032142	0.00001
NM_005522.5(HOXA1):c.813C>T (p.Thr271=)	rs1435619628	0.00001
NM_005522.4(HOXA1):c.-89T>C	rs1783820241
NM_005522.5(HOXA1):c.*1058T>A	rs1311098639
NM_005522.5(HOXA1):c.*183G>A	rs186304469
NM_005522.5(HOXA1):c.*183G>C	rs186304469
NM_005522.5(HOXA1):c.*232G>A	rs1783762321
NM_005522.5(HOXA1):c.*281C>G	rs1783761584
NM_005522.5(HOXA1):c.*820A>G	rs1336175696
NM_005522.5(HOXA1):c.-26C>A	rs764712990
NM_005522.5(HOXA1):c.-86C>A	rs964954049
NM_005522.5(HOXA1):c.122C>T (p.Ala41Val)	rs1783812000
NM_005522.5(HOXA1):c.294C>G (p.Ser98Arg)	rs377149193
NM_005522.5(HOXA1):c.63G>A (p.Gly21=)	rs1331715096

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