ClinVar Miner

Variants in gene ZFYVE26 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 24
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HGVS dbSNP gnomAD frequency
NM_015346.4(ZFYVE26):c.4854C>T (p.Leu1618=) rs151287975 0.00246
NM_015346.4(ZFYVE26):c.773G>A (p.Arg258Gln) rs150230201 0.00113
NM_015346.4(ZFYVE26):c.1945G>A (p.Val649Met) rs144790966 0.00107
NM_015346.4(ZFYVE26):c.5401G>A (p.Ala1801Thr) rs138965635 0.00056
NM_015346.4(ZFYVE26):c.5260G>A (p.Ala1754Thr) rs146968463 0.00045
NM_015346.4(ZFYVE26):c.2799C>T (p.Leu933=) rs146793500 0.00044
NM_015346.4(ZFYVE26):c.2396C>T (p.Thr799Met) rs200179480 0.00014
NM_015346.4(ZFYVE26):c.2742C>T (p.Ser914=) rs140577908 0.00013
NM_015346.4(ZFYVE26):c.879G>A (p.Ser293=) rs199794711 0.00013
NM_015346.4(ZFYVE26):c.5321-3C>T rs376234357 0.00011
NM_015346.4(ZFYVE26):c.4293G>C (p.Gln1431His) rs373740172 0.00008
NM_015346.4(ZFYVE26):c.403G>A (p.Val135Met) rs771937001 0.00003
NM_015346.4(ZFYVE26):c.7317C>T (p.Asp2439=) rs147321202 0.00003
NM_015346.4(ZFYVE26):c.1272-10T>C rs773153713 0.00001
NM_015346.4(ZFYVE26):c.1819G>A (p.Gly607Arg) rs142015707 0.00001
NM_015346.4(ZFYVE26):c.6870A>G (p.Ser2290=) rs766701632 0.00001
NM_015346.4(ZFYVE26):c.3017G>A (p.Arg1006Gln)
NM_015346.4(ZFYVE26):c.3248_3253del (p.Leu1083_Ser1084del) rs761454264
NM_015346.4(ZFYVE26):c.4197C>T (p.Thr1399=) rs35018134
NM_015346.4(ZFYVE26):c.4502C>T (p.Thr1501Met) rs201034965
NM_015346.4(ZFYVE26):c.475G>C (p.Asp159His)
NM_015346.4(ZFYVE26):c.5622-10_5622-9del rs768978705
NM_015346.4(ZFYVE26):c.715C>T (p.Leu239=)
NM_015346.4(ZFYVE26):c.7371+6C>G rs894907950

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