Variant (rsID / SNP)

rs6468171

rs6468171 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAK16, TTI2. Location: chromosome 8, position 33,356,074. The table records no clinical significance for this variant.

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Reference-table entries

MAK16Not classified

Variant type: missense_variant
Chromosome / position: 8:33356074
HGVS: NM_032509.4,c.830A>G,p.Gln277Arg
Allele change: Missense_Q277R

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.