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Variant (rsID / SNP)

rs4516060

DHX37

rs4516060 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DHX37. Location: chromosome 12, position 125,438,516. The table records no clinical significance for this variant.

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Reference-table entries

DHX37Not classified
Variant type
missense_variant
Chromosome / position
12:125438516
HGVS
NM_032656.4,c.2605A>G,p.Ser869Gly
Allele change
Missense_S869G

Public references

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