Variant (rsID / SNP)

rs1572912

rs1572912 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D13. Location: chromosome 9, position 131,565,554. The table records no clinical significance for this variant.

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Reference-table entries

TBC1D13Not classified

Variant type: missense_variant
Chromosome / position: 9:131565554
HGVS: NM_018201.5,c.569T>C,p.Val190Ala
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.