Variant (rsID / SNP)

rs2270941

rs2270941 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DHDH. Location: chromosome 19, position 49,438,363. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DHDHNot classified

Variant type: missense_variant
Chromosome / position: 19:49438363
HGVS: NM_014475.4,c.197G>A,p.Ser66Asn
Allele change: Missense_S66N

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.