List of variants in gene combination HOXA11, LOC107126281 reported as uncertain significance for Radioulnar synostosis with amegakaryocytic thrombocytopenia 1

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005523.6(HOXA11):c.396G>C (p.Arg132Ser)	rs143812636	0.00052
NM_005523.6(HOXA11):c.152T>A (p.Leu51Gln)	rs150569316	0.00023
NM_005523.6(HOXA11):c.10G>C (p.Asp4His)	rs752525999	0.00001
NM_005523.6(HOXA11):c.328A>C (p.Ser110Arg)
NM_005523.6(HOXA11):c.380A>G (p.Tyr127Cys)
NM_005523.6(HOXA11):c.451C>A (p.Pro151Thr)	rs1783832681
NM_005523.6(HOXA11):c.531GGC[7] (p.Ala183_Thr184insAlaAla)

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