Variant (rsID / SNP)

rs77238711

rs77238711 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF536. Location: chromosome 19, position 31,039,669. Clinical significance in the table: Benign.

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Reference-table entries

ZNF536Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:31039669
Cytoband: 19q12
HGVS: NM_014717.3(ZNF536):c.3143C>T (p.Ala1048Val)
Allele change: Missense_A1048V

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.