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Variant (rsID / SNP)

rs1774266

HYDIN

rs1774266 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HYDIN. Location: chromosome 16, position 70,993,566. The table records no clinical significance for this variant.

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Reference-table entries

HYDINNot classified
Variant type
synonymous_variant
Chromosome / position
16:70993566
HGVS
NM_001270974.2,c.6126T>C,p.His2042His
Allele change
Synonymous_H2042H

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.