ClinVar Miner

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

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_014425.5(INVS):c.1038G>A (p.Ser346=) rs372355067
NM_014425.5(INVS):c.114T>C (p.Ser38=) rs114056499
NM_014425.5(INVS):c.1560C>T (p.Asn520=) rs201691547
NM_014425.5(INVS):c.1674C>A (p.Ala558=) rs143140689
NM_014425.5(INVS):c.1896G>A (p.Val632=) rs746617240
NM_014425.5(INVS):c.1925A>G (p.Lys642Arg) rs116314059
NM_014425.5(INVS):c.2247G>A (p.Arg749=) rs769950635
NM_014425.5(INVS):c.2310C>T (p.His770=) rs116606949
NM_014425.5(INVS):c.2402G>A (p.Gly801Glu) rs76868679
NM_014425.5(INVS):c.276A>C (p.Gly92=) rs1554724084
NM_014425.5(INVS):c.3017-5T>G rs201018893
NM_014425.5(INVS):c.900C>T (p.Asn300=) rs752481190
NM_014425.5(INVS):c.913G>A (p.Val305Ile) rs116438342

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