Variant (rsID / SNP)

rs2732481

rs2732481 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF641. Location: chromosome 12, position 48,736,985. The table records no clinical significance for this variant.

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Reference-table entries

ZNF641Not classified

Variant type: missense_variant
Chromosome / position: 12:48736985
HGVS: NM_152320.3,c.1088A>C,p.Gln363Pro
Allele change: Missense_Q363P

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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