ClinVar Miner

List of variants in gene EGF studied for Hypomagnesemia 4, renal

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 123
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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.*1118A>C rs183204371
NM_001963.6(EGF):c.*1220G>A
NM_001963.6(EGF):c.*1222A>G rs11569149
NM_001963.6(EGF):c.*1244T>C rs7653900
NM_001963.6(EGF):c.*1265T>A rs537226223
NM_001963.6(EGF):c.*1266T>A rs11569150
NM_001963.6(EGF):c.*1283C>T rs193265825
NM_001963.6(EGF):c.*1305T>C
NM_001963.6(EGF):c.*1356T>C rs749675346
NM_001963.6(EGF):c.*1435T>C
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.*393T>C rs3733625
NM_001963.6(EGF):c.*411A>G rs886058998
NM_001963.6(EGF):c.*42C>T
NM_001963.6(EGF):c.*446C>T rs534531408
NM_001963.6(EGF):c.*479T>C rs548932345
NM_001963.6(EGF):c.*483C>T rs11569146
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.-102G>A rs11568848
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.-382A>G rs4444903
NM_001963.6(EGF):c.-424G>A
NM_001963.6(EGF):c.-447G>A rs56399752
NM_001963.6(EGF):c.-60C>T
NM_001963.6(EGF):c.-78A>G
NM_001963.6(EGF):c.1066+10G>C rs76435576
NM_001963.6(EGF):c.1066+12A>G
NM_001963.6(EGF):c.1095T>C (p.His365=) rs11568937
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.1190-10T>C
NM_001963.6(EGF):c.1258T>G (p.Leu420Val)
NM_001963.6(EGF):c.127+14T>A
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.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.1723G>A (p.Gly575Arg) rs115396821
NM_001963.6(EGF):c.1725-12C>A rs11568990
NM_001963.6(EGF):c.1789A>G (p.Ile597Val) rs41482245
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.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.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.2124G>A (p.Met708Ile) rs2237051
NM_001963.6(EGF):c.2223A>G (p.Gly741=)
NM_001963.6(EGF):c.2297C>T (p.Ser766Leu)
NM_001963.6(EGF):c.2298G>A (p.Ser766=) rs41491249
NM_001963.6(EGF):c.2337G>A (p.Thr779=)
NM_001963.6(EGF):c.2351A>T (p.Asp784Val) rs11569017
NM_001963.6(EGF):c.2362C>T (p.Leu788=) rs376855018
NM_001963.6(EGF):c.2433G>A (p.Val811=) rs149396988
NM_001963.6(EGF):c.2525T>C (p.Met842Thr) rs11569046
NM_001963.6(EGF):c.2608+14G>A rs886058992
NM_001963.6(EGF):c.2609-5C>A rs74379237
NM_001963.6(EGF):c.264C>T (p.Ile88=) rs11568885
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.2759A>T (p.Glu920Val) rs4698803
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.3118G>A (p.Val1040Met) rs75935899
NM_001963.6(EGF):c.3162C>G (p.Ala1054=) rs548762791
NM_001963.6(EGF):c.3209C>T (p.Pro1070Leu) rs121434567
NM_001963.6(EGF):c.3251C>G (p.Ala1084Gly) rs11569111
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.3521C>A (p.Thr1174Asn) rs28592692
NM_001963.6(EGF):c.3530G>C (p.Gly1177Ala) rs140730971
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.47G>C (p.Ser16Thr) rs200394315
NM_001963.6(EGF):c.556G>C (p.Asp186His) rs28553469
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.769G>C (p.Asp257His) rs11568911
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)
NM_001963.6(EGF):c.875T>A (p.Leu292His) rs35191533
NM_001963.6(EGF):c.940+11G>A rs4698756

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