Variant (rsID / SNP)

rs41307788

rs41307788 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MASP2. Location: chromosome 1, position 11,105,542. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MASP2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:11105542
Cytoband: 1p36.22
HGVS: NM_006610.4(MASP2):c.467G>A (p.Cys156Tyr)
Allele change: Missense_C156Y

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.