Variant (rsID / SNP)

rs6741778

rs6741778 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EVA1A. Location: chromosome 2, position 75,720,664. The table records no clinical significance for this variant.

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Reference-table entries

EVA1ANot classified

Variant type: synonymous_variant
Chromosome / position: 2:75720664
HGVS: NM_001135032.2,c.157C>T,p.Leu53Leu
Allele change: Synonymous_L53L

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.