ClinVar Miner

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

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_000890.5(KCNJ5):c.*1091G>A rs565178107
NM_000890.5(KCNJ5):c.*1216C>T rs566376081
NM_000890.5(KCNJ5):c.*121G>T rs78979538
NM_000890.5(KCNJ5):c.*1302C>T rs552826605
NM_000890.5(KCNJ5):c.*1310C>T rs537850039
NM_000890.5(KCNJ5):c.*34G>T rs116494206
NM_000890.5(KCNJ5):c.*449A>T rs115414355
NM_000890.5(KCNJ5):c.*547G>A rs114896724
NM_000890.5(KCNJ5):c.*759C>T rs75453162
NM_000890.5(KCNJ5):c.*936C>T rs77525858
NM_000890.5(KCNJ5):c.*960G>C rs186315097
NM_000890.5(KCNJ5):c.*96G>A rs77092337
NM_000890.5(KCNJ5):c.*977T>C rs181648220
NM_000890.5(KCNJ5):c.-63G>C rs557063967
NM_000890.5(KCNJ5):c.1159G>C (p.Gly387Arg) rs199830292
NM_000890.5(KCNJ5):c.121C>T (p.Arg41Cys) rs115012103
NM_000890.5(KCNJ5):c.1254G>A (p.Ser418=) rs528463709
NM_000890.5(KCNJ5):c.273C>T (p.Leu91=) rs146853795
NM_000890.5(KCNJ5):c.430A>G (p.Ile144Val) rs369703183
NM_000890.5(KCNJ5):c.744G>A (p.Glu248=) rs144040058
NM_000890.5(KCNJ5):c.957G>A (p.Arg319=) rs192889782

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