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Variant (rsID / SNP)

rs1176537

ETV3L

rs1176537 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ETV3L. Location: chromosome 1, position 157,062,696. The table records no clinical significance for this variant.

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Reference-table entries

ETV3LNot classified
Variant type
synonymous_variant
Chromosome / position
1:157062696
HGVS
NM_001004341.2,c.831C>A,p.Leu277Leu
Allele change
Synonymous_L277L

Public references

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