Variant (rsID / SNP)

rs11666105

rs11666105 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DHDH. Location: chromosome 19, position 49,445,817. The table records no clinical significance for this variant.

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Reference-table entries

DHDHNot classified

Variant type: missense_variant
Chromosome / position: 19:49445817
HGVS: NM_014475.4,c.740T>C,p.Val247Ala
Allele change: Missense_V247A

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.