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Variant (rsID / SNP)

rs3795886

KCNE4

rs3795886 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNE4. Location: chromosome 2, position 223,917,629. The table records no clinical significance for this variant.

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Reference-table entries

KCNE4Not classified
Variant type
synonymous_variant
Chromosome / position
2:223917629
HGVS
NM_080671.4,c.81C>T,p.Gly27Gly
Allele change
Synonymous_G78G

Public references

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