ClinVar Miner

List of variants in gene RTN2 reported by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_005619.5(RTN2):c.1593C>T (p.Ala531=) rs148630935 0.00720
NM_005619.5(RTN2):c.792C>A (p.Phe264Leu) rs61745812 0.00699
NM_005619.5(RTN2):c.1143G>A (p.Ala381=) rs45532933 0.00572
NM_005619.5(RTN2):c.444C>G (p.Gly148=) rs139232850 0.00550
NM_005619.5(RTN2):c.351A>G (p.Gln117=) rs144028452 0.00450
NM_005619.5(RTN2):c.285A>G (p.Glu95=) rs146004780 0.00381
NM_005619.5(RTN2):c.1168G>A (p.Gly390Ser) rs143937661 0.00242
NM_005619.5(RTN2):c.1274G>A (p.Arg425Gln) rs35461805 0.00177
NM_005619.5(RTN2):c.1312C>T (p.Arg438Cys) rs148270789 0.00049
NM_005619.5(RTN2):c.1630G>A (p.Ala544Thr) rs201387324 0.00015
NM_005619.5(RTN2):c.858T>A (p.Val286=) rs376174832 0.00010
NM_005619.5(RTN2):c.1210G>A (p.Val404Met) rs200512597 0.00009
NM_005619.5(RTN2):c.174C>T (p.Thr58=) rs199928834 0.00008
NM_005619.5(RTN2):c.1618T>C (p.Ser540Pro) rs779865623 0.00006
NM_005619.5(RTN2):c.1476C>G (p.Pro492=) rs748824542 0.00004
NM_005619.5(RTN2):c.1366G>A (p.Val456Met) rs533022763 0.00002
NM_005619.5(RTN2):c.1322C>T (p.Ser441Leu) rs755367786 0.00001
NM_005619.5(RTN2):c.389C>T (p.Ala130Val) rs745409162 0.00001
NM_005619.5(RTN2):c.79+6T>A rs749104931 0.00001
NM_005619.5(RTN2):c.916G>A (p.Val306Ile) rs181791404 0.00001
NM_005619.5(RTN2):c.1497+2T>C rs1421302939
NM_005619.5(RTN2):c.184C>G (p.Leu62Val)
NM_005619.5(RTN2):c.35-5C>G rs757800024
NM_005619.5(RTN2):c.455G>C (p.Arg152Pro)
NM_005619.5(RTN2):c.745G>A (p.Glu249Lys) rs761286207
NM_005619.5(RTN2):c.770A>C (p.Asp257Ala) rs1555798140
NM_005619.5(RTN2):c.834A>G (p.Leu278=) rs1555798029

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