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Variant (rsID / SNP)

rs7586970

TFPI

rs7586970 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TFPI. Location: chromosome 2, position 188,343,497. The table records no clinical significance for this variant.

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Reference-table entries

TFPINot classified
Variant type
missense_variant
Chromosome / position
2:188343497
HGVS
NM_001032281.4,c.662A>G,p.Asn221Ser
Allele change
Silent

Associated conditions / phenotypes

Vascular Disease

Public references

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