ClinVar Miner

List of variants in gene SLC7A9 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (962):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_014270.5(SLC7A9):c.*79T>C rs2287884
NM_014270.5(SLC7A9):c.-172T>A rs2287876
NM_014270.5(SLC7A9):c.-39C>T rs11084677
NM_014270.5(SLC7A9):c.1143C>T (p.Ala381=) rs2287881
NM_014270.5(SLC7A9):c.399C>T (p.Ser133=) rs35170371
NM_014270.5(SLC7A9):c.411T>C (p.Cys137=) rs12150890
NM_014270.5(SLC7A9):c.425T>C (p.Val142Ala) rs12150889
NM_014270.5(SLC7A9):c.478+10T>C rs6510300
NM_014270.5(SLC7A9):c.507C>T (p.Ser169=) rs11084673
NM_014270.5(SLC7A9):c.604+10G>A rs11084672
NM_014270.5(SLC7A9):c.667C>A (p.Leu223Met) rs1007160
NM_014270.5(SLC7A9):c.687C>T (p.Leu229=) rs1007161

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