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Variant (rsID / SNP)

rs2234079

ETV7

rs2234079 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ETV7. Location: chromosome 6, position 36,339,136. The table records no clinical significance for this variant.

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Reference-table entries

ETV7Not classified
Variant type
missense_variant
Chromosome / position
6:36339136
HGVS
NM_016135.4,c.635C>T,p.Pro212Leu
Allele change
Missense_P157L

Associated conditions / phenotypes

Silent|Missense_P131L|Missense_P153L

Public references

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