ClinVar Miner

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

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 21
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HGVS dbSNP gnomAD frequency
NM_001723.7(DST):c.7765A>G (p.Ile2589Val) rs150191284 0.02534
NM_001723.7(DST):c.3809A>G (p.Lys1270Arg) rs35497571 0.02037
NM_001374736.1(DST):c.15584G>A (p.Cys5195Tyr) rs57472891 0.01957
NM_001374736.1(DST):c.17923-10A>G rs116504133 0.01889
NM_001374736.1(DST):c.3495-17T>C rs74865335 0.01174
NM_001374736.1(DST):c.20997G>A (p.Leu6999=) rs187652380 0.00781
NM_001374736.1(DST):c.13820C>A (p.Pro4607His) rs138967674 0.00744
NM_001374736.1(DST):c.3557G>A (p.Ser1186Asn) rs139350480 0.00572
NM_001723.7(DST):c.5780A>G (p.His1927Arg) rs12209266 0.00441
NM_001723.7(DST):c.5909T>C (p.Phe1970Ser) rs141573097 0.00280
NM_001374736.1(DST):c.14461A>C (p.Asn4821His) rs139089184 0.00260
NM_001374736.1(DST):c.2256A>T (p.Ser752=) rs113432929 0.00225
NM_001374736.1(DST):c.60C>G (p.Phe20Leu) rs150003298 0.00220
NM_001374736.1(DST):c.22916C>T (p.Ala7639Val) rs201429821 0.00178
NM_001374736.1(DST):c.2350C>G (p.Pro784Ala) rs151271595 0.00152
NM_001723.7(DST):c.7135G>A (p.Ala2379Thr) rs140192373 0.00140
NM_001723.7(DST):c.6582A>C (p.Ala2194=) rs149007397 0.00115
NM_001374736.1(DST):c.5059-17C>G rs190803185 0.00089
NM_001374736.1(DST):c.2042G>A (p.Arg681His) rs143101723 0.00058
NM_001374736.1(DST):c.3126G>A (p.Lys1042=) rs76795414 0.00004
NM_001374736.1(DST):c.14311-6T>G

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