Variant (rsID / SNP)

rs76754832

rs76754832 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DHRS4. Location: chromosome 14, position 24,435,144. The table records no clinical significance for this variant.

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Reference-table entries

DHRS4Not classified

Variant type: missense_variant
Chromosome / position: 14:24435144
HGVS: NM_001282987.2,c.412C>T,p.Arg138Trp
Allele change: Synonymous_G161G

Associated conditions / phenotypes

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.