ClinVar Miner

List of variants in gene RET reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.3187+47T>C rs2075912 0.84041
NM_020975.6(RET):c.1296A>G (p.Ala432=) rs1800860 0.74268
NM_020975.6(RET):c.867+48A>G rs2435352 0.37996
NM_020975.6(RET):c.337+9G>A rs2435351 0.20840
NM_020975.6(RET):c.2608-24G>A rs2472737 0.20232
NM_020975.6(RET):c.2284+47C>T rs760466 0.18873
NM_020975.6(RET):c.2712C>G (p.Ser904=) rs1800863 0.17043
NM_020975.6(RET):c.2071G>A (p.Gly691Ser) rs1799939 0.16948
NM_020975.6(RET):c.2508C>T (p.Ser836=) rs1800862 0.03791
NM_020975.6(RET):c.1264-5C>T rs9282835 0.02749
NM_020975.6(RET):c.2944C>T (p.Arg982Cys) rs17158558 0.01651
NM_020975.6(RET):c.868-18G>A rs57098408 0.00960
NM_020975.6(RET):c.375C>A (p.Val125=) rs1800859 0.00877
NM_020975.6(RET):c.166C>A (p.Leu56Met) rs145633958 0.00310
NM_020975.6(RET):c.1336G>C (p.Gly446Arg) rs115423919 0.00238
NM_020975.6(RET):c.1465G>A (p.Asp489Asn) rs9282834 0.00106
NM_020975.6(RET):c.833C>A (p.Thr278Asn) rs35118262 0.00056
NM_020975.6(RET):c.2976G>A (p.Pro992=) rs528823385 0.00048
NM_020975.6(RET):c.200G>A (p.Arg67His) rs192489011 0.00036
NM_020975.6(RET):c.2088G>A (p.Ser696=) rs150329150 0.00023
NM_020975.6(RET):c.1064-18T>C rs546346375 0.00001
NM_020975.6(RET):c.1840GAG[2] (p.Glu616del) rs377767399

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