ClinVar Miner

List of variants in gene GLB1 reported as benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_000404.4(GLB1):c.*182A>G rs76762176
NM_000404.4(GLB1):c.*354T>C rs12167
NM_000404.4(GLB1):c.1032T>C (p.Thr344=) rs199927127
NM_000404.4(GLB1):c.1209C>G (p.Pro403=) rs528690108
NM_000404.4(GLB1):c.1233+8T>C rs13093698
NM_000404.4(GLB1):c.1306C>T (p.Leu436Phe) rs34421970
NM_000404.4(GLB1):c.1561= (p.Cys521=) rs4302331
NM_000404.4(GLB1):c.1561T>C (p.Cys521Arg) rs4302331
NM_000404.4(GLB1):c.1577G>A (p.Gly526Asp) rs147332381
NM_000404.4(GLB1):c.1594A>G (p.Ser532Gly) rs73826339
NM_000404.4(GLB1):c.1824G>C (p.Leu608=) rs77226678
NM_000404.4(GLB1):c.1833G>A (p.Ser611=) rs201755284
NM_000404.4(GLB1):c.325C>T (p.Arg109Trp) rs35289681
NM_000404.4(GLB1):c.458-11T>C rs34204221
NM_000404.4(GLB1):c.734-112T>C
NM_000404.4(GLB1):c.734-99G>T
NM_000404.4(GLB1):c.756C>T (p.Phe252=) rs142326197
NM_000404.4(GLB1):c.76-4426C>T
NM_000404.4(GLB1):c.792+10G>T rs79518579
NM_000404.4(GLB1):c.792+18G>A
NM_000404.4(GLB1):c.793-14dup
NM_000404.4(GLB1):c.955+60A>G rs12632196

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