ClinVar Miner

List of variants in gene CNNM2 reported as uncertain significance for Hypomagnesemia 6, renal

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Total variants: 27
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HGVS dbSNP
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.*519G>A rs0
NM_017649.5(CNNM2):c.*53G>A rs886046672
NM_017649.5(CNNM2):c.*606G>C rs0
NM_017649.5(CNNM2):c.*686T>A rs886046674
NM_017649.5(CNNM2):c.*690C>T rs886046675
NM_017649.5(CNNM2):c.*811A>G rs886046676
NM_017649.5(CNNM2):c.*834C>T rs886046677
NM_017649.5(CNNM2):c.-65G>A rs886046668
NM_017649.5(CNNM2):c.1263C>G (p.Thr421=) rs0
NM_017649.5(CNNM2):c.1621+21dup rs0
NM_017649.5(CNNM2):c.1764C>T (p.Tyr588=) rs747058788
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.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.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.296C>G (p.Thr99Ser) rs0
NM_017649.5(CNNM2):c.49C>G (p.Gln17Glu) rs886046669
NM_017649.5(CNNM2):c.849C>T (p.Asp283=) rs0

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