ClinVar Miner

List of variants reported as benign for Renal hypomagnesemia 2 by Illumina Laboratory Services, Illumina

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001680.5(FXYD2):c.*176T>G rs11999 0.27930
NM_001680.5(FXYD2):c.*1C>T rs869789 0.13143
NM_001680.5(FXYD2):c.-10A>G rs12279985 0.02777
NM_001680.5(FXYD2):c.*105C>T rs78017409 0.01539
NM_001680.5(FXYD2):c.45C>T (p.Asp15=) rs35705701 0.01109
NM_001680.5(FXYD2):c.*6+6C>A rs11827585 0.00767
NM_001680.5(FXYD2):c.*215G>A rs41304349 0.00511
NM_001680.5(FXYD2):c.195G>A (p.Glu65=) rs144519777 0.00419
NM_001680.5(FXYD2):c.28G>A (p.Gly10Ser) rs146614981 0.00083
NM_001680.5(FXYD2):c.76G>A (p.Val26Ile) rs149878562 0.00079
NM_001680.5(FXYD2):c.126C>T (p.Leu42=) rs144279659 0.00040
NM_001680.5(FXYD2):c.*71G>A rs565539331 0.00009
NM_001680.5(FXYD2):c.90C>T (p.Gly30=) rs373687268 0.00004
NM_001680.5(FXYD2):c.*78C>A rs114952534
NM_001680.5(FXYD2):c.198G>T (p.Pro66=) rs149353193

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