Variant (rsID / SNP)

rs2267808

rs2267808 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AMPH. Location: chromosome 7, position 38,468,463. The table records no clinical significance for this variant.

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Reference-table entries

AMPHNot classified

Variant type: intron_variant
Chromosome / position: 7:38468463
HGVS: NM_001635.4,c.1182+979G>A
Allele change: Silent

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.