Variant (rsID / SNP)

rs115718556

rs115718556 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LTBP4. Location: chromosome 19, position 41,133,653. Clinical significance in the table: Benign.

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Reference-table entries

LTBP4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:41133653
Cytoband: 19q13.2
HGVS: NM_001042545.2(LTBP4):c.4410C>T (p.Cys1470=)
Allele change: Missense_A1500V

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.