Variant (rsID / SNP)

rs17779352

rs17779352 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AHR. Location: chromosome 7, position 17,349,626. The table records no clinical significance for this variant.

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Reference-table entries

AHRNot classified

Variant type: synonymous_variant
Chromosome / position: 7:17349626
HGVS: NM_001621.5,c.132T>C,p.Asn44Asn
Allele change: Synonymous_N44N

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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