List of variants in gene combination FXYD2, FXYD6-FXYD2 reported as benign for Renal hypomagnesemia 2

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

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	0.01653
NM_001680.5(FXYD2):c.45C>T (p.Asp15=)	rs35705701	0.01144
NM_001680.5(FXYD2):c.*6+6C>A	rs11827585	0.00767
NM_001680.5(FXYD2):c.*215G>A	rs41304349	0.00461
NM_001680.5(FXYD2):c.195G>A (p.Glu65=)	rs144519777	0.00367
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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