Variant (rsID / SNP)

rs11574819

rs11574819 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP3K14. Location: chromosome 17, position 43,364,638. Clinical significance in the table: Benign.

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Reference-table entries

MAP3K14Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:43364638
Cytoband: 17q21.31
HGVS: NM_003954.5(MAP3K14):c.419G>A (p.Ser140Asn)
Allele change: Missense_S140N

Associated conditions / phenotypes

NIK deficiency

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.