Variant (rsID / SNP)

rs11732887

rs11732887 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D14. Location: chromosome 4, position 6,956,059. The table records no clinical significance for this variant.

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Reference-table entries

TBC1D14Not classified

Variant type: missense_variant
Chromosome / position: 4:6956059
HGVS: NM_001330638.2,c.32T>C,p.Met11Thr
Allele change: Silent

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.