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Variant (rsID / SNP)

rs6034464

KIF16B

rs6034464 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF16B. Location: chromosome 20, position 16,359,567. The table records no clinical significance for this variant.

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Reference-table entries

KIF16BNot classified
Variant type
missense_variant
Chromosome / position
20:16359567
HGVS
NM_001199866.2,c.3080T>C,p.Met1027Thr
Allele change
Missense_M1027T

Public references

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