Variant (rsID / SNP)

rs5909299

rs5909299 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP3K15. The table records no clinical significance for this variant.

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Reference-table entries

MAP3K15Not classified

Variant type: missense_variant
HGVS: NM_001001671.4,c.574G>A,p.Ala192Thr
Allele change: Missense_A192T

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.