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Variant (rsID / SNP)

rs1889323

SVEP1

rs1889323 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SVEP1. Location: chromosome 9, position 113,209,195. The table records no clinical significance for this variant.

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Reference-table entries

SVEP1Not classified
Variant type
missense_variant
Chromosome / position
9:113209195
HGVS
NM_153366.4,c.4246A>C,p.Lys1416Gln
Allele change
Missense_K1416Q

Public references

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