Variant (rsID / SNP)

rs30386

rs30386 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D9B. Location: chromosome 5, position 179,290,845. The table records no clinical significance for this variant.

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Reference-table entries

TBC1D9BNot classified

Variant type: missense_variant
Chromosome / position: 5:179290845
HGVS: NM_198868.3,c.3356A>C,p.Lys1119Thr
Allele change: Missense_K1119T

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.