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Variant (rsID / SNP)

rs1138294

MAP3K6

rs1138294 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP3K6. Location: chromosome 1, position 27,688,633. The table records no clinical significance for this variant.

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Reference-table entries

MAP3K6Not classified
Variant type
missense_variant
Chromosome / position
1:27688633
HGVS
NM_004672.5,c.1364C>T,p.Thr455Ile
Allele change
Missense_T455I

Public references

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