Variant (rsID / SNP)

rs7255596

rs7255596 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF837. Location: chromosome 19, position 58,879,976. The table records no clinical significance for this variant.

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Reference-table entries

ZNF837Not classified

Variant type: missense_variant
Chromosome / position: 19:58879976
HGVS: NM_138466.2,c.724G>A,p.Ala242Thr
Allele change: Missense_A242T

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.