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Variant (rsID / SNP)

rs12484074

ZC3H7B

rs12484074 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZC3H7B. Location: chromosome 22, position 41,752,747. The table records no clinical significance for this variant.

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Reference-table entries

ZC3H7BNot classified
Variant type
synonymous_variant
Chromosome / position
22:41752747
HGVS
NM_017590.6,c.2616G>A,p.Thr872Thr
Allele change
Synonymous_T872T

Public references

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