ClinVar Miner

Variants in gene DNAAF2 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 10
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NM_018139.2(DNAAF2):c.1406G>A (p.Cys469Tyr) rs150737854
NM_018139.2(DNAAF2):c.144C>A (p.Asn48Lys) rs116185352
NM_018139.2(DNAAF2):c.1463G>A (p.Gly488Glu) rs200121200
NM_018139.2(DNAAF2):c.1494G>A (p.Ser498=) rs2985688
NM_018139.2(DNAAF2):c.1626G>C (p.Arg542=) rs35763780
NM_018139.2(DNAAF2):c.1851C>T (p.Asn617=) rs147090213
NM_018139.2(DNAAF2):c.1953A>G (p.Pro651=) rs34352773
NM_018139.2(DNAAF2):c.2388C>T (p.His796=) rs140997181
NM_018139.2(DNAAF2):c.561C>T (p.Thr187=) rs529083217
NM_018139.2(DNAAF2):c.728A>C (p.Glu243Ala) rs112044935

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