ClinVar Miner

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

Included ClinVar conditions (1030):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_001008216.2(GALE):c.*195T>C
NM_001008216.2(GALE):c.-77+241C>G rs566996145
NM_001008216.2(GALE):c.330C>T (p.Thr110=) rs377557637
NM_001008216.2(GALE):c.369G>A (p.Gly123=) rs138148991
NM_001008216.2(GALE):c.372G>A (p.Val124=) rs550325454
NM_001008216.2(GALE):c.423C>T (p.Tyr141=) rs138518245
NM_001008216.2(GALE):c.643-7C>T rs771926683
NM_001008216.2(GALE):c.770A>G (p.Lys257Arg) rs28940884
NM_001008216.2(GALE):c.772C>T (p.Leu258=) rs147618796
NM_001008216.2(GALE):c.873+13G>C rs760941
NM_001008216.2(GALE):c.873+7C>A rs746500876
NM_001008216.2(GALE):c.879G>A (p.Pro293=) rs142332521
NM_001008216.2(GALE):c.912G>A (p.Val304=) rs143694860
NM_001008216.2(GALE):c.956G>A (p.Gly319Glu) rs28940885

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