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Variant (rsID / SNP)

rs79607350

HYDIN

rs79607350 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HYDIN. Location: chromosome 16, position 70,843,712. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

HYDINConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:70843712
Cytoband
16q22.2
HGVS
NM_001270974.2(HYDIN):c.14857C>T (p.Arg4953Trp)
Allele change
Missense_R4953W

Public references

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