Variant (rsID / SNP)

rs61749398

rs61749398 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VWF. Location: chromosome 12, position 6,128,614. Clinical significance in the table: Pathogenic.

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Reference-table entries

VWFPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 12:6128614
Cytoband: 12p13.31
HGVS: NM_000552.5(VWF):c.3970G>A (p.Gly1324Ser)
Allele change: Missense_G1324S

Associated conditions / phenotypes

von Willebrand disease type 2M

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.