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Variant (rsID / SNP)

rs7118900

ANKK1

rs7118900 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKK1. Location: chromosome 11, position 113,266,821. The table records no clinical significance for this variant.

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Reference-table entries

ANKK1Not classified
Variant type
missense_variant
Chromosome / position
11:113266821
HGVS
NM_178510.2,c.715G>A,p.Ala239Thr
Allele change
Missense_A239T

Associated conditions / phenotypes

Opioid Addiction

Public references

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