Variant (rsID / SNP)

rs5988

rs5988 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F13A1. Location: chromosome 6, position 6,152,137. Clinical significance in the table: Benign.

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Reference-table entries

F13A1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:6152137
Cytoband: 6p25.1
HGVS: NM_000129.4(F13A1):c.1954G>C (p.Glu652Gln)
Allele change: Missense_E652Q

Associated conditions / phenotypes

Factor XIII, A subunit, deficiency of

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.