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Variant (rsID / SNP)

rs1139583

MAP4K4

rs1139583 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP4K4. Location: chromosome 2, position 102,472,459. The table records no clinical significance for this variant.

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Reference-table entries

MAP4K4Not classified
Variant type
synonymous_variant
Chromosome / position
2:102472459
HGVS
NM_001395002.1,c.1254A>G,p.Glu418Glu
Allele change
Synonymous_E418E

Public references

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