Variant (rsID / SNP)

rs141145402

rs141145402 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MASP2. Location: chromosome 1, position 11,106,642. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MASP2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:11106642
Cytoband: 1p36.22
HGVS: NM_006610.4(MASP2):c.383C>T (p.Thr128Met)
Allele change: Missense_T128M

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.