ClinVar Miner

List of variants in gene CNNM2 studied for Hypomagnesemia 6, renal

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Total variants: 61
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HGVS dbSNP
NM_017649.5(CNNM2):c.*1162G>A rs148051463
NM_017649.5(CNNM2):c.*1246G>C rs553490290
NM_017649.5(CNNM2):c.*159G>C rs0
NM_017649.5(CNNM2):c.*205G>A rs886046673
NM_017649.5(CNNM2):c.*310C>T rs0
NM_017649.5(CNNM2):c.*311G>A rs376027544
NM_017649.5(CNNM2):c.*34C>T rs0
NM_017649.5(CNNM2):c.*3C>T rs2296568
NM_017649.5(CNNM2):c.*455C>T rs3740389
NM_017649.5(CNNM2):c.*519G>A rs0
NM_017649.5(CNNM2):c.*528G>A rs3740388
NM_017649.5(CNNM2):c.*52C>T rs367767821
NM_017649.5(CNNM2):c.*53G>A rs886046672
NM_017649.5(CNNM2):c.*543A>G rs0
NM_017649.5(CNNM2):c.*606G>C rs0
NM_017649.5(CNNM2):c.*619A>G rs138807273
NM_017649.5(CNNM2):c.*686T>A rs886046674
NM_017649.5(CNNM2):c.*690C>T rs886046675
NM_017649.5(CNNM2):c.*794G>A rs41287480
NM_017649.5(CNNM2):c.*811A>G rs886046676
NM_017649.5(CNNM2):c.*834C>T rs886046677
NM_017649.5(CNNM2):c.*879G>A rs1046411
NM_017649.5(CNNM2):c.*891G>T rs185818969
NM_017649.5(CNNM2):c.*904G>C rs145537350
NM_017649.5(CNNM2):c.-110A>T rs555951352
NM_017649.5(CNNM2):c.-65G>A rs886046668
NM_017649.5(CNNM2):c.1128C>T (p.Ile376=) rs0
NM_017649.5(CNNM2):c.1134C>T (p.Leu378=) rs2297785
NM_017649.5(CNNM2):c.113G>A (p.Arg38Gln) rs76057237
NM_017649.5(CNNM2):c.117del (p.Ile40fs) rs1564803221
NM_017649.5(CNNM2):c.1263C>G (p.Thr421=) rs0
NM_017649.5(CNNM2):c.1515C>T (p.Pro505=) rs144140948
NM_017649.5(CNNM2):c.1621+21dup rs0
NM_017649.5(CNNM2):c.1622-6C>T rs74464353
NM_017649.5(CNNM2):c.1703C>T (p.Thr568Ile) rs387906975
NM_017649.5(CNNM2):c.1764C>T (p.Tyr588=) rs747058788
NM_017649.5(CNNM2):c.1842T>C (p.Ser614=) rs2275271
NM_017649.5(CNNM2):c.2004C>T (p.Asn668=) rs0
NM_017649.5(CNNM2):c.2012C>T (p.Ala671Val) rs375262395
NM_017649.5(CNNM2):c.2073+14T>C rs184406418
NM_017649.5(CNNM2):c.210G>A (p.Glu70=) rs886046670
NM_017649.5(CNNM2):c.2125G>T (p.Ala709Ser) rs0
NM_017649.5(CNNM2):c.2188A>G (p.Thr730Ala) rs886046671
NM_017649.5(CNNM2):c.2190C>T (p.Thr730=) rs0
NM_017649.5(CNNM2):c.2310C>T (p.Ala770=) rs943037
NM_017649.5(CNNM2):c.2355G>C (p.Ser785=) rs0
NM_017649.5(CNNM2):c.2385G>T (p.Ser795=) rs0
NM_017649.5(CNNM2):c.2400G>A (p.Ser800=) rs0
NM_017649.5(CNNM2):c.2430G>T (p.Gln810His) rs0
NM_017649.5(CNNM2):c.2544C>T (p.Asp848=) rs35647154
NM_017649.5(CNNM2):c.296C>G (p.Thr99Ser) rs0
NM_017649.5(CNNM2):c.342G>T (p.Thr114=) rs375416482
NM_017649.5(CNNM2):c.411C>G (p.Gly137=) rs0
NM_017649.5(CNNM2):c.49C>G (p.Gln17Glu) rs886046669
NM_017649.5(CNNM2):c.564C>T (p.Ser188=) rs117691462
NM_017649.5(CNNM2):c.604G>A (p.Ala202Thr) rs75800852
NM_017649.5(CNNM2):c.621C>T (p.Ser207=) rs0
NM_017649.5(CNNM2):c.801C>T (p.Cys267=) rs367789750
NM_017649.5(CNNM2):c.849C>T (p.Asp283=) rs0
NM_017649.5(CNNM2):c.903C>T (p.Tyr301=) rs140279763
NM_017649.5(CNNM2):c.90C>T (p.Arg30=) rs202027427

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