ClinVar Miner

List of variants reported as likely benign for intestinal hypomagnesemia 1

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_017662.4(TRPM6):c.-167A>C rs77048628 0.02299
NM_017662.4(TRPM6):c.-163A>G rs73538241 0.02297
NM_017662.5(TRPM6):c.2428C>T (p.Leu810=) rs55956641 0.01104
NM_017662.5(TRPM6):c.4569A>T (p.Thr1523=) rs150409948 0.00610
NM_017662.5(TRPM6):c.5550A>G (p.Gln1850=) rs35618857 0.00349
NM_017662.5(TRPM6):c.*1222C>T rs190131362 0.00291
NM_017662.5(TRPM6):c.511G>A (p.Gly171Arg) rs150874152 0.00278
NM_017662.5(TRPM6):c.633T>C (p.Gly211=) rs144221623 0.00259
NM_017662.5(TRPM6):c.390G>A (p.Glu130=) rs140236011 0.00257
NM_017662.5(TRPM6):c.1014G>T (p.Met338Ile) rs56155062 0.00211
NM_017662.5(TRPM6):c.3095-17A>T rs78719948 0.00150
NM_017662.5(TRPM6):c.*1160C>T rs563649179 0.00118
NM_017662.5(TRPM6):c.*670A>C rs144874847 0.00072
NM_017662.5(TRPM6):c.5424T>C (p.Pro1808=) rs140812450 0.00068
NM_017662.5(TRPM6):c.2811G>A (p.Ala937=) rs145231172 0.00067
NM_017662.5(TRPM6):c.*1784A>G rs143290917 0.00055
NM_017662.5(TRPM6):c.4719G>A (p.Ala1573=) rs41304234 0.00035
NM_017662.5(TRPM6):c.*96C>G rs369609402 0.00034
NM_017662.5(TRPM6):c.5481C>T (p.Cys1827=) rs150963618 0.00034
NM_017662.5(TRPM6):c.2649T>C (p.Ala883=) rs373991938 0.00016
NM_017662.5(TRPM6):c.3288C>T (p.His1096=) rs138479474 0.00015
NM_017662.5(TRPM6):c.5709G>A (p.Leu1903=) rs143047185 0.00014
NM_017662.5(TRPM6):c.3501T>C (p.Cys1167=) rs966765338 0.00007
NM_017662.5(TRPM6):c.705C>T (p.Leu235=) rs373729845 0.00007
NM_017662.5(TRPM6):c.5685C>A (p.Thr1895=) rs757763880 0.00006
NM_017662.5(TRPM6):c.622C>A (p.Pro208Thr) rs755626959 0.00006
NM_017662.5(TRPM6):c.1207+18G>A rs371897441 0.00004
NM_017662.5(TRPM6):c.2118C>T (p.Thr706=) rs149238868 0.00004
NM_017662.5(TRPM6):c.2478G>A (p.Pro826=) rs375316759 0.00004
NM_017662.5(TRPM6):c.5415C>A (p.Ser1805=) rs150150126 0.00002
NM_017662.5(TRPM6):c.3094+19C>T rs532772332 0.00001
NM_017662.5(TRPM6):c.*235C>T rs527880339
NM_017662.5(TRPM6):c.*710AT[3] rs201267884
NM_017662.5(TRPM6):c.*919G>T rs371692085
NM_017662.5(TRPM6):c.1224G>A (p.Ala408=) rs141597109
NM_017662.5(TRPM6):c.886G>A (p.Gly296Ser)

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