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Variant (rsID / SNP)

rs1111032

KCNK15

rs1111032 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNK15. Location: chromosome 20, position 43,378,770. The table records no clinical significance for this variant.

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Reference-table entries

KCNK15Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
20:43378770
HGVS
NM_022358.4,c.284A>G,p.Glu95Gly
Allele change
Missense_E95G

Public references

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