ClinVar Miner

List of variants reported as benign for Hypomagnesemia 4, renal

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_001963.6(EGF):c.*1222A>G rs11569149
NM_001963.6(EGF):c.*1244T>C rs7653900
NM_001963.6(EGF):c.*1435T>C
NM_001963.6(EGF):c.*393T>C rs3733625
NM_001963.6(EGF):c.*483C>T rs11569146
NM_001963.6(EGF):c.-382A>G rs4444903
NM_001963.6(EGF):c.-424G>A
NM_001963.6(EGF):c.1066+10G>C rs76435576
NM_001963.6(EGF):c.1095T>C (p.His365=) rs11568937
NM_001963.6(EGF):c.1292G>A (p.Arg431Lys) rs11568943
NM_001963.6(EGF):c.1313-10G>T rs11568952
NM_001963.6(EGF):c.1380A>G (p.Glu460=) rs11568953
NM_001963.6(EGF):c.1725-12C>A rs11568990
NM_001963.6(EGF):c.1789A>G (p.Ile597Val) rs41482245
NM_001963.6(EGF):c.1914C>G (p.Ser638Arg) rs11568992
NM_001963.6(EGF):c.1977C>T (p.Cys659=) rs11568993
NM_001963.6(EGF):c.2073A>G (p.Ala691=) rs2302135
NM_001963.6(EGF):c.2124G>A (p.Met708Ile) rs2237051
NM_001963.6(EGF):c.2298G>A (p.Ser766=) rs41491249
NM_001963.6(EGF):c.2351A>T (p.Asp784Val) rs11569017
NM_001963.6(EGF):c.2525T>C (p.Met842Thr) rs11569046
NM_001963.6(EGF):c.2609-5C>A rs74379237
NM_001963.6(EGF):c.264C>T (p.Ile88=) rs11568885
NM_001963.6(EGF):c.2759A>T (p.Glu920Val) rs4698803
NM_001963.6(EGF):c.3118G>A (p.Val1040Met) rs75935899
NM_001963.6(EGF):c.3251C>G (p.Ala1084Gly) rs11569111
NM_001963.6(EGF):c.451C>T (p.His151Tyr) rs9991664
NM_001963.6(EGF):c.46A>C (p.Ser16Arg) rs11568849
NM_001963.6(EGF):c.556G>C (p.Asp186His) rs28553469
NM_001963.6(EGF):c.769G>C (p.Asp257His) rs11568911
NM_001963.6(EGF):c.875T>A (p.Leu292His) rs35191533
NM_001963.6(EGF):c.940+11G>A rs4698756

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