Variant (rsID / SNP)

rs1044095

rs1044095 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF91. Location: chromosome 19, position 23,545,250. The table records no clinical significance for this variant.

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Reference-table entries

ZNF91Not classified

Variant type: synonymous_variant
Chromosome / position: 19:23545250
HGVS: NM_003430.4,c.531T>C,p.Thr177Thr
Allele change: Synonymous_T145T

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.