Variant (rsID / SNP)

rs4699735

rs4699735 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADH6. Location: chromosome 4, position 100,140,306. The table records no clinical significance for this variant.

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Reference-table entries

ADH6Not classified

Variant type: missense_variant
Chromosome / position: 4:100140306
HGVS: NM_001102470.2,c.4T>A,p.Cys2Ser
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.