ClinVar Miner

List of variants in gene FECH reported as pathogenic 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: 17
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HGVS dbSNP
NM_000140.3(FECH):c.1078_1137del rs879255507
NM_000140.3(FECH):c.195_314del rs786205246
NM_000140.3(FECH):c.68_194del rs786205247
NM_000140.3(FECH):c.[1224T>A;1225C>T;1231T>G]
NM_000140.4(FECH):c.1077+1G>A rs786205245
NM_000140.4(FECH):c.1085T>G (p.Val362Gly) rs118204040
NM_000140.4(FECH):c.1136del (p.Lys379fs) rs764466739
NM_000140.4(FECH):c.1137+3A>G rs202147607
NM_000140.4(FECH):c.1250T>C (p.Phe417Ser) rs118204039
NM_000140.4(FECH):c.163G>T (p.Gly55Cys) rs3848519
NM_000140.4(FECH):c.314+2T>G rs149067146
NM_000140.4(FECH):c.315-48T>C rs2272783
NM_000140.4(FECH):c.553G>A (p.Ala185Thr) rs397514476
NM_000140.4(FECH):c.580_584del (p.Tyr194fs) rs786205248
NM_000140.4(FECH):c.68-23C>T rs2269219
NM_000140.4(FECH):c.801G>A (p.Met267Ile) rs118204037
NM_000140.4(FECH):c.820G>A (p.Asp274Asn) rs146269992

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