Variant (rsID / SNP)

rs2254344

rs2254344 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF180. Location: chromosome 19, position 45,001,619. The table records no clinical significance for this variant.

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Reference-table entries

ZNF180Not classified

Variant type: intron_variant
Chromosome / position: 19:45001619
HGVS: NM_013256.7,c.44-195G>A
Allele change: Silent

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.