ClinVar Miner

Variants in gene ZSWIM6 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 21
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HGVS dbSNP gnomAD frequency
NM_020928.2(ZSWIM6):c.1334-15C>T rs143225117 0.01725
NM_020928.2(ZSWIM6):c.1729C>T (p.Arg577Cys) rs116036211 0.00361
NM_020928.2(ZSWIM6):c.1906G>A (p.Val636Met) rs140760439 0.00337
NM_020928.2(ZSWIM6):c.243G>T (p.Ala81=) rs553592342 0.00333
NM_020928.2(ZSWIM6):c.3119G>A (p.Arg1040His) rs192222164 0.00054
NM_020928.2(ZSWIM6):c.1472A>G (p.Asn491Ser) rs201912422 0.00048
NM_020928.2(ZSWIM6):c.636G>A (p.Ala212=) rs565326403 0.00048
NM_020928.2(ZSWIM6):c.582C>T (p.Ala194=) rs746876878 0.00046
NM_020928.2(ZSWIM6):c.2142A>G (p.Lys714=) rs769830528 0.00044
NM_020928.2(ZSWIM6):c.2013A>G (p.Glu671=) rs369326083 0.00029
NM_020928.2(ZSWIM6):c.3039G>A (p.Ala1013=) rs374621238 0.00021
NM_020928.2(ZSWIM6):c.1893T>C (p.His631=) rs757310729 0.00016
NM_020928.2(ZSWIM6):c.2890G>A (p.Val964Ile) rs774718702 0.00004
NM_020928.2(ZSWIM6):c.151GCG[7] (p.Ala56dup) rs779283808
NM_020928.2(ZSWIM6):c.222C>T (p.Pro74=) rs757648079
NM_020928.2(ZSWIM6):c.2788G>A (p.Val930Ile) rs748023376
NM_020928.2(ZSWIM6):c.477GGCCGCAACCTCGGC[1] (p.162TSAAA[1]) rs541338051
NM_020928.2(ZSWIM6):c.522CGC[11] (p.Ala184_Gly185insAla) rs1262946696
NM_020928.2(ZSWIM6):c.57CGG[4] (p.Gly25_Gly26del) rs565100893
NM_020928.2(ZSWIM6):c.57CGG[5] (p.Gly26del) rs565100893
NM_020928.2(ZSWIM6):c.83GCG[7] (p.Gly33dup) rs528020839

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