ClinVar Miner

List of variants reported as uncertain significance for Hypomagnesemia 4, renal

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 77
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HGVS dbSNP
NM_001963.6(EGF):c.*1001C>G rs765122805
NM_001963.6(EGF):c.*1005A>G
NM_001963.6(EGF):c.*1068G>A
NM_001963.6(EGF):c.*107C>T rs886058996
NM_001963.6(EGF):c.*1220G>A
NM_001963.6(EGF):c.*1265T>A rs537226223
NM_001963.6(EGF):c.*1305T>C
NM_001963.6(EGF):c.*1356T>C rs749675346
NM_001963.6(EGF):c.*157G>A rs190671898
NM_001963.6(EGF):c.*184A>C rs886058997
NM_001963.6(EGF):c.*18A>G rs745325610
NM_001963.6(EGF):c.*201A>C rs539507877
NM_001963.6(EGF):c.*361T>C rs542979630
NM_001963.6(EGF):c.*411A>G rs886058998
NM_001963.6(EGF):c.*479T>C rs548932345
NM_001963.6(EGF):c.*561G>C rs11569147
NM_001963.6(EGF):c.*67A>G rs572682450
NM_001963.6(EGF):c.*835G>A rs886058999
NM_001963.6(EGF):c.*929G>A rs112147938
NM_001963.6(EGF):c.*937G>T
NM_001963.6(EGF):c.-127A>C rs886058990
NM_001963.6(EGF):c.-140A>G rs543779474
NM_001963.6(EGF):c.-228G>C
NM_001963.6(EGF):c.-265G>T rs886058989
NM_001963.6(EGF):c.-270T>G
NM_001963.6(EGF):c.-273T>C
NM_001963.6(EGF):c.-283G>C rs886058988
NM_001963.6(EGF):c.-342C>G
NM_001963.6(EGF):c.-361C>G
NM_001963.6(EGF):c.-60C>T
NM_001963.6(EGF):c.1066+12A>G
NM_001963.6(EGF):c.1097G>A (p.Gly366Asp)
NM_001963.6(EGF):c.1137C>T (p.Tyr379=) rs971946479
NM_001963.6(EGF):c.1180C>T (p.Arg394Ter) rs369702571
NM_001963.6(EGF):c.1258T>G (p.Leu420Val)
NM_001963.6(EGF):c.127+14T>A
NM_001963.6(EGF):c.1404C>T (p.Asp468=)
NM_001963.6(EGF):c.1416T>A (p.Asp472Glu)
NM_001963.6(EGF):c.1491T>C (p.His497=) rs377445081
NM_001963.6(EGF):c.1575+6G>A rs148355596
NM_001963.6(EGF):c.1575+6G>T
NM_001963.6(EGF):c.1602G>A (p.Lys534=) rs140682556
NM_001963.6(EGF):c.1684G>C (p.Val562Leu)
NM_001963.6(EGF):c.1818T>C (p.His606=) rs139266578
NM_001963.6(EGF):c.1821A>G (p.Pro607=)
NM_001963.6(EGF):c.1851A>G (p.Thr617=)
NM_001963.6(EGF):c.2082G>C (p.Glu694Asp)
NM_001963.6(EGF):c.2088T>C (p.Tyr696=) rs375886742
NM_001963.6(EGF):c.2115A>G (p.Pro705=) rs762377539
NM_001963.6(EGF):c.2223A>G (p.Gly741=)
NM_001963.6(EGF):c.2337G>A (p.Thr779=)
NM_001963.6(EGF):c.2362C>T (p.Leu788=) rs376855018
NM_001963.6(EGF):c.2608+14G>A rs886058992
NM_001963.6(EGF):c.2682T>G (p.Gly894=)
NM_001963.6(EGF):c.2742T>C (p.Asp914=) rs886058993
NM_001963.6(EGF):c.2755G>A (p.Gly919Arg) rs886058994
NM_001963.6(EGF):c.2760G>A (p.Glu920=) rs760507781
NM_001963.6(EGF):c.2858-11G>T rs370698699
NM_001963.6(EGF):c.2940C>T (p.His980=) rs140319442
NM_001963.6(EGF):c.3006-11T>G
NM_001963.6(EGF):c.3073G>T (p.Ala1025Ser) rs149056615
NM_001963.6(EGF):c.3110C>T (p.Ala1037Val) rs572990451
NM_001963.6(EGF):c.3162C>G (p.Ala1054=) rs548762791
NM_001963.6(EGF):c.3286C>T (p.Pro1096Ser)
NM_001963.6(EGF):c.3292-7T>C rs200524686
NM_001963.6(EGF):c.3346G>T (p.Gly1116Cys) rs886058995
NM_001963.6(EGF):c.3371-12T>C
NM_001963.6(EGF):c.3371-4A>G rs41468451
NM_001963.6(EGF):c.3530G>C (p.Gly1177Ala) rs140730971
NM_001963.6(EGF):c.47G>C (p.Ser16Thr) rs200394315
NM_001963.6(EGF):c.57T>C (p.Ser19=) rs767958539
NM_001963.6(EGF):c.662G>C (p.Arg221Thr)
NM_001963.6(EGF):c.731C>A (p.Pro244Gln)
NM_001963.6(EGF):c.742A>G (p.Asn248Asp)
NM_001963.6(EGF):c.791G>A (p.Trp264Ter) rs867950317
NM_001963.6(EGF):c.803C>A (p.Thr268Lys)
NM_001963.6(EGF):c.835G>A (p.Asp279Asn)

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