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Variant (rsID / SNP)

rs3732235

ZNF638

rs3732235 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF638. Location: chromosome 2, position 71,631,109. The table records no clinical significance for this variant.

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Reference-table entries

ZNF638Not classified
Variant type
missense_variant
Chromosome / position
2:71631109
HGVS
NM_001014972.3,c.2939A>G,p.Asn980Ser
Allele change
Missense_N980S

Public references

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