ClinVar Miner

List of variants reported as likely benign for Renal hypomagnesemia 2

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_001680.5(FXYD2):c.110C>A (p.Ala37Asp) rs138991613 0.00053
NM_001680.5(FXYD2):c.126C>T (p.Leu42=) rs144279659 0.00040
NM_001680.5(FXYD2):c.183C>T (p.Ile61=) rs201669990 0.00011
NM_001680.5(FXYD2):c.114C>T (p.Phe38=) rs151172706 0.00009
NM_001680.5(FXYD2):c.90C>T (p.Gly30=) rs373687268 0.00004
NM_001680.5(FXYD2):c.198G>A (p.Pro66=) rs149353193
NM_001680.5(FXYD2):c.198G>T (p.Pro66=) rs149353193

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