Variant (rsID / SNP)

rs9995922

rs9995922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DTHD1. Location: chromosome 4, position 36,317,970. The table records no clinical significance for this variant.

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Reference-table entries

DTHD1Not classified

Variant type: synonymous_variant
Chromosome / position: 4:36317970
HGVS: NM_001170700.3,c.2202T>C,p.Ser734Ser
Allele change: Synonymous_S444S

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.