Variant (rsID / SNP)

rs7793993

rs7793993 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VWDE. Location: chromosome 7, position 12,417,407. The table records no clinical significance for this variant.

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Reference-table entries

VWDENot classified

Variant type: missense_variant
Chromosome / position: 7:12417407
HGVS: NM_001135924.3,c.1019G>A,p.Gly340Asp
Allele change: Missense_G185D

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.