ClinVar Miner

List of variants in gene MGP studied for bone disorder

Included ClinVar conditions (1350):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_000900.5(MGP):c.304A>G (p.Thr102Ala) rs4236 0.41895
NM_000900.5(MGP):c.-63G>A rs1800801 0.32542
NM_000900.5(MGP):c.*140T>C rs148802642 0.00331
NM_000900.5(MGP):c.157A>G (p.Lys53Glu) rs1801716 0.00329
NM_000900.5(MGP):c.115A>C (p.Asn39His) rs145210821 0.00260
NM_000900.5(MGP):c.23C>T (p.Ala8Val) rs142330429 0.00171
NM_000900.5(MGP):c.*27T>G rs80337043 0.00164
NM_000900.4(MGP):c.-117C>T rs569710471 0.00071
NM_000900.5(MGP):c.207T>C (p.Asn69=) rs186013880 0.00056
NM_000900.4(MGP):c.-66C>A rs150994762 0.00043
NM_000900.5(MGP):c.234T>C (p.Leu78=) rs149084241 0.00034
NM_000900.5(MGP):c.198C>T (p.His66=) rs151158281 0.00024
NM_000900.5(MGP):c.62-2A>G rs112518413 0.00001
NM_000900.5(MGP):c.84T>C (p.Ser28=) rs886049107 0.00001
NM_000900.5(MGP):c.*176C>G rs935518014
NM_000900.5(MGP):c.237C>T (p.Cys79=) rs886049106
NM_000900.5(MGP):c.43del (p.Ala14_Val15insTer) rs730880321
NM_000900.5(MGP):c.46G>A (p.Val16Ile) rs868750856
NM_000900.5(MGP):c.62-18dup rs11393307
NM_000900.5(MGP):c.62-9del rs11393307
NM_000900.5(MGP):c.62A>T (p.Glu21Val)
NM_000900.5(MGP):c.77T>C (p.Met26Thr) rs754107566
NM_000900.5(MGP):c.87T>A (p.Tyr29Ter) rs730880322
NM_000900.5(MGP):c.94+1G>A rs111320759

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