Variant (rsID / SNP)

rs114749335

rs114749335 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LTBP4. Location: chromosome 19, position 41,114,207. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

LTBP4Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:41114207
Cytoband: 19q13.2
HGVS: NM_001042545.2(LTBP4):c.1238G>A (p.Gly413Asp)
Allele change: Missense_G443D

Associated conditions / phenotypes

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.