ClinVar Miner

List of variants in gene KCNJ5 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP
NM_000890.5(KCNJ5):c.*1063G>A rs2846696
NM_000890.5(KCNJ5):c.*1168C>G rs1137937
NM_000890.5(KCNJ5):c.*1338C>A rs6590358
NM_000890.5(KCNJ5):c.*1338del rs144472942
NM_000890.5(KCNJ5):c.*378dup rs397799938
NM_000890.5(KCNJ5):c.*410C>T rs2846675
NM_000890.5(KCNJ5):c.*528C>T rs3867250
NM_000890.5(KCNJ5):c.*779G>T rs4373934
NM_000890.5(KCNJ5):c.*804G>T rs2604204
NM_000890.5(KCNJ5):c.*861_*865GTTTT[7] rs36205004
NM_000890.5(KCNJ5):c.*928C>T rs7925056
NM_000890.5(KCNJ5):c.*976G>A rs7102315
NM_000890.5(KCNJ5):c.171T>C (p.Ser57=) rs6590357
NM_000890.5(KCNJ5):c.810T>G (p.Leu270=) rs7118824
NM_000890.5(KCNJ5):c.834T>C (p.His278=) rs7118833
NM_000890.5(KCNJ5):c.844C>G (p.Gln282Glu) rs7102584
NM_000890.5(KCNJ5):c.937+7C>T rs45516097
NM_000890.5(KCNJ5):c.938-10G>A rs4937391

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