Variant (rsID / SNP)

rs141002143

rs141002143 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBX15. Location: chromosome 1, position 119,441,695. Clinical significance in the table: Likely benign.

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Reference-table entries

TBX15Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:119441695
Cytoband: 1p12
HGVS: NM_001330677.2(TBX15):c.980G>A (p.Arg327His)
Allele change: Missense_R327H

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.