Variant (rsID / SNP)

rs56392418

rs56392418 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MASP2. Location: chromosome 1, position 11,106,648. Clinical significance in the table: Benign.

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Reference-table entries

MASP2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:11106648
Cytoband: 1p36.22
HGVS: NM_006610.4(MASP2):c.377C>T (p.Pro126Leu)
Allele change: Missense_P126L

Associated conditions / phenotypes

Immunodeficiency due to MASP-2 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.