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Variant (rsID / SNP)

rs1058768

TINAG

rs1058768 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TINAG. Location: chromosome 6, position 54,186,147. The table records no clinical significance for this variant.

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Reference-table entries

TINAGNot classified
Variant type
missense_variant
Chromosome / position
6:54186147
HGVS
NM_014464.4,c.472T>C,p.Ser158Pro
Allele change
Missense_S158P

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.