Variant (rsID / SNP)

rs62621193

rs62621193 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARID4A. Location: chromosome 14, position 58,832,019. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ARID4AConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 14:58832019
Cytoband: 14q23.1
HGVS: NM_002892.4(ARID4A):c.3211+1G>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.