ClinVar Miner

List of variants in gene INVS reported as 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: 23
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NM_014425.5(INVS):c.-110T>G rs7024375
NM_014425.5(INVS):c.102C>T (p.Ile34=) rs115640267
NM_014425.5(INVS):c.1235-5T>C rs2245216
NM_014425.5(INVS):c.1284T>C (p.His428=) rs77465715
NM_014425.5(INVS):c.1374C>A (p.Thr458=) rs114912725
NM_014425.5(INVS):c.1704G>A (p.Gly568=) rs114645869
NM_014425.5(INVS):c.1948G>C (p.Ala650Pro) rs147452898
NM_014425.5(INVS):c.1980A>G (p.Gly660=) rs139314036
NM_014425.5(INVS):c.2116A>G (p.Arg706Gly) rs116222916
NM_014425.5(INVS):c.2193C>T (p.Gly731=) rs148758887
NM_014425.5(INVS):c.2402G>A (p.Gly801Glu) rs76868679
NM_014425.5(INVS):c.2412T>C (p.Ser804=) rs2787374
NM_014425.5(INVS):c.2604C>T (p.Ser868=) rs751765105
NM_014425.5(INVS):c.2719C>A (p.Arg907=) rs267607185
NM_014425.5(INVS):c.274-15_274-14del rs61147858
NM_014425.5(INVS):c.2803C>T (p.His935Tyr) rs139768159
NM_014425.5(INVS):c.3017-5T>G rs201018893
NM_014425.5(INVS):c.3027C>T (p.His1009=) rs201136636
NM_014425.5(INVS):c.3182dup (p.Asn1061fs) rs760013326
NM_014425.5(INVS):c.725C>T (p.Ser242Leu) rs2491097
NM_014425.5(INVS):c.740A>G (p.Asn247Ser) rs41312220
NM_014425.5(INVS):c.913G>A (p.Val305Ile) rs116438342

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