Variant (rsID / SNP)

rs971074

rs971074 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADH7. Location: chromosome 4, position 100,341,861. The table records no clinical significance for this variant.

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Reference-table entries

ADH7Not classified

Variant type: synonymous_variant
Chromosome / position: 4:100341861
HGVS: NM_001166504.2,c.714G>A,p.Arg238Arg
Allele change: Synonymous_R238R

Associated conditions / phenotypes

Adrenal Cortical Carcinoma|Adrenocortical Carcinoma, Hereditary|Adrenal Cortical Adenocarcinoma

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.