ClinVar Miner

List of variants studied for Renal hypomagnesemia 2

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Total variants: 35
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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.110C>A (p.Ala37Asp) rs138991613 0.00053
NM_001680.5(FXYD2):c.126C>T (p.Leu42=) rs144279659 0.00040
NM_001680.5(FXYD2):c.176+3G>A rs200472357 0.00035
NM_001680.5(FXYD2):c.*124T>A rs756608243 0.00031
NM_001680.5(FXYD2):c.183C>T (p.Ile61=) rs201669990 0.00014
NM_001680.5(FXYD2):c.176G>A (p.Arg59Lys) rs139816783 0.00012
NM_001680.5(FXYD2):c.*149A>G rs41313497 0.00011
NM_001680.5(FXYD2):c.*71G>A rs565539331 0.00009
NM_001680.5(FXYD2):c.114C>T (p.Phe38=) rs151172706 0.00009
NM_001680.5(FXYD2):c.176+6C>T rs368170451 0.00006
NM_001680.5(FXYD2):c.90C>T (p.Gly30=) rs373687268 0.00004
NM_001680.5(FXYD2):c.173G>A (p.Arg58His) rs761860028 0.00002
NM_001680.5(FXYD2):c.53C>T (p.Pro18Leu) rs763425417 0.00002
NM_001680.5(FXYD2):c.65-1G>A rs767357379 0.00001
NM_001680.5(FXYD2):c.*78C>A rs114952534
NM_001680.5(FXYD2):c.121G>A (p.Gly41Arg) rs28938168
NM_001680.5(FXYD2):c.186T>A (p.Asn62Lys)
NM_001680.5(FXYD2):c.198G>A (p.Pro66=) rs149353193
NM_001680.5(FXYD2):c.198G>T (p.Pro66=) rs149353193
NM_001680.5(FXYD2):c.25G>T (p.Gly9Cys) rs2134106055
NM_001680.5(FXYD2):c.36C>G (p.Pro12=) rs778901593
NM_001680.5(FXYD2):c.41G>A (p.Gly14Glu)
NM_001680.5(FXYD2):c.49G>A (p.Asp17Asn)
NM_001680.5(FXYD2):c.52C>G (p.Pro18Ala)
NM_001680.5(FXYD2):c.52C>T (p.Pro18Ser)

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