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Variant (rsID / SNP)

rs710446

KNG1

rs710446 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KNG1. Location: chromosome 3, position 186,459,927. The table records no clinical significance for this variant.

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Reference-table entries

KNG1Not classified
Variant type
missense_variant
Chromosome / position
3:186459927
HGVS
NM_001102416.3,c.1742T>C,p.Ile581Thr
Allele change
Silent

Associated conditions / phenotypes

Thrombophilia Due to Thrombin Defect|Thrombosis|Alzheimer Disease|Thrombophilia|Stroke, Ischemic|Microvascular Complications of Diabetes 6|Microvascular Complications of Diabetes 4|Microvascular Complications of Diabetes 3|Microvascular Complications of Diabetes 7

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.