ClinVar Miner

List of variants reported as likely benign for Hypomagnesemia 4, renal

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ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_001963.6(EGF):c.*1118A>C rs183204371
NM_001963.6(EGF):c.*1266T>A rs11569150
NM_001963.6(EGF):c.*1283C>T rs193265825
NM_001963.6(EGF):c.*42C>T
NM_001963.6(EGF):c.*446C>T rs534531408
NM_001963.6(EGF):c.-102G>A rs11568848
NM_001963.6(EGF):c.-447G>A rs56399752
NM_001963.6(EGF):c.-78A>G
NM_001963.6(EGF):c.1190-10T>C
NM_001963.6(EGF):c.1723G>A (p.Gly575Arg) rs115396821
NM_001963.6(EGF):c.2297C>T (p.Ser766Leu)
NM_001963.6(EGF):c.2433G>A (p.Val811=) rs149396988
NM_001963.6(EGF):c.3521C>A (p.Thr1174Asn) rs28592692

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