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Variant (rsID / SNP)

rs2071192

EVPL

rs2071192 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EVPL. Location: chromosome 17, position 74,014,668. The table records no clinical significance for this variant.

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Reference-table entries

EVPLNot classified
Variant type
missense_variant
Chromosome / position
17:74014668
HGVS
NM_001320747.2,c.1298A>G,p.Gln433Arg
Allele change
Missense_Q433R

Public references

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