ClinVar Miner

List of variants in gene WHRN reported as uncertain significance by GeneDx

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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_015404.4(WHRN):c.19G>C (p.Gly7Arg) rs572671060 0.00141
NM_015404.4(WHRN):c.1149C>T (p.Thr383=) rs149558159 0.00098
NM_015404.4(WHRN):c.2438C>T (p.Thr813Met) rs143728180 0.00078
NM_015404.4(WHRN):c.2027C>G (p.Pro676Arg) rs139279977 0.00067
NM_015404.4(WHRN):c.2510G>A (p.Arg837His) rs55749855 0.00053
NM_015404.4(WHRN):c.1148C>A (p.Thr383Asn) rs147283064 0.00052
NM_015404.4(WHRN):c.2101G>C (p.Gly701Arg) rs111373159 0.00047
NM_015404.4(WHRN):c.995G>A (p.Arg332Gln) rs139193948 0.00045
NM_015404.4(WHRN):c.2417C>T (p.Pro806Leu) rs149897775 0.00036
NM_015404.4(WHRN):c.1381A>C (p.Met461Leu) rs144878400 0.00022
NM_015404.4(WHRN):c.2183G>A (p.Arg728His) rs138767834 0.00021
NM_015404.4(WHRN):c.2060C>T (p.Pro687Leu) rs534523640 0.00014
NM_015404.4(WHRN):c.1049G>A (p.Arg350Gln) rs529362314 0.00011
NM_015404.4(WHRN):c.998G>A (p.Ser333Asn) rs200073414 0.00011
NM_015404.4(WHRN):c.1999G>A (p.Ala667Thr) rs202161016 0.00010
NM_015404.4(WHRN):c.2390A>G (p.Glu797Gly) rs375820423 0.00010
NM_015404.4(WHRN):c.1222C>A (p.Pro408Thr) rs368241259 0.00009
NM_015404.4(WHRN):c.1349G>A (p.Arg450His) rs200377723 0.00007
NM_015404.4(WHRN):c.2093T>A (p.Val698Glu) rs201184915 0.00007
NM_015404.4(WHRN):c.1597G>A (p.Gly533Ser) rs752659496 0.00006
NM_015404.4(WHRN):c.695A>C (p.His232Pro) rs533374297 0.00006
NM_015404.4(WHRN):c.73G>T (p.Gly25Cys) rs774198237 0.00005
NM_015404.4(WHRN):c.2246C>T (p.Thr749Met) rs767100303 0.00004
NM_015404.4(WHRN):c.2474C>G (p.Thr825Ser) rs200422759 0.00004
NM_015404.4(WHRN):c.35C>T (p.Ser12Leu) rs760261757 0.00003
NM_015404.4(WHRN):c.1757C>T (p.Pro586Leu) rs771542666 0.00002
NM_015404.4(WHRN):c.2299G>T (p.Asp767Tyr) rs200583397 0.00002
NM_015404.4(WHRN):c.314T>C (p.Leu105Pro) rs751083422 0.00002
NM_015404.4(WHRN):c.1378G>A (p.Val460Ile) rs373389359 0.00001
NM_015404.4(WHRN):c.1591A>C (p.Ser531Arg) rs1217731688 0.00001
NM_015404.4(WHRN):c.1810A>G (p.Arg604Gly) rs373975842 0.00001
NM_015404.4(WHRN):c.2056C>A (p.Pro686Thr) rs201690920 0.00001
NM_015404.4(WHRN):c.2189A>G (p.Asp730Gly) rs772190770 0.00001
NM_015404.4(WHRN):c.2219C>T (p.Ala740Val) rs976736112 0.00001
NM_015404.4(WHRN):c.2453G>A (p.Arg818His) rs762248099 0.00001
NM_015404.4(WHRN):c.2611A>G (p.Thr871Ala) rs779001003 0.00001
NM_015404.4(WHRN):c.1577G>C (p.Gly526Ala)
NM_015404.4(WHRN):c.1619C>T (p.Ser540Leu)
NM_015404.4(WHRN):c.1627-10C>A
NM_015404.4(WHRN):c.1850C>T (p.Ser617Leu) rs150146590
NM_015404.4(WHRN):c.1930G>C (p.Asp644His) rs201707482
NM_015404.4(WHRN):c.2309A>T (p.Glu770Val) rs1168947739
NM_015404.4(WHRN):c.2351C>G (p.Ser784Cys)
NM_015404.4(WHRN):c.2492A>G (p.Glu831Gly) rs781538079
NM_015404.4(WHRN):c.2644C>A (p.Arg882Ser) rs150586098
NM_015404.4(WHRN):c.2644C>T (p.Arg882Cys) rs150586098
NM_015404.4(WHRN):c.2701A>C (p.Thr901Pro)
NM_015404.4(WHRN):c.616A>G (p.Lys206Glu)
NM_015404.4(WHRN):c.683A>G (p.Tyr228Cys)

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