SERPINH1, -656C-T

Variation ID: Help
8664
Review status: Help
(0/4) no assertion criteria provided0 stars out of maximum of 4 stars

Interpretation Help

Clinical significance:
Pathogenic
Last evaluated:
Sep 5, 2006
Number of submission(s):
1
Condition(s):
Preterm premature rupture of membranes[MedGen - OMIM]
See supporting ClinVar records

Allele(s) Help

SERPINH1, -656C-T

Allele ID:
23703
Variant type:
single nucleotide variant
Cytogenetic location:
11q13.5
Other names:
  • -656C-T
Links:
OMIM: 600943.0001

Variant frequency in dbGaP Help

No dbGaP data has been submitted for this variant.

Assertion and evidence details

Germline

Clinical significance
(Last evaluated)
Review status
(Assertion method)
Collection methodCondition(s)
(Mode of inheritance)
OriginCitationsSubmitter - Study nameSubmission accession
Pathogenic
(Sep 5, 2006)
no assertion criteria providedliterature only
  • Preterm premature rupture of membranes[MedGen | OMIM]
germlineOMIMSCV000029413.1
SubmitterFamiliesIndividualsAllele originEthnicityGeographic originCitations and DatabasesDescription
OMIMnot providednot providedgermlinenot providednot providednot provided
SubmitterAllele originIndividualsPhenotypes (Affected status)EthnicityGeographic originCitationsDescription

Last Updated: Apr 7, 2017