Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs1573496

ADH7

rs1573496 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADH7. Location: chromosome 4, position 100,349,669. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

ADH7Not classified
Variant type
missense_variant
Chromosome / position
4:100349669
HGVS
NM_001166504.2,c.299G>C,p.Gly100Ala
Allele change
Missense_G100A

Associated conditions / phenotypes

Oral Cancer|Squamous Cell Carcinoma|Squamous Cell Carcinoma, Head and Neck|Esophageal Cancer|Oral Cavity Cancer

Public references

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