Variant (rsID / SNP)

rs78712333

rs78712333 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARID2. Location: chromosome 12, position 46,246,611. Clinical significance in the table: Likely benign.

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Reference-table entries

ARID2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:46246611
Cytoband: 12q12
HGVS: NM_152641.4(ARID2):c.4705G>A (p.Ala1569Thr)
Allele change: Missense_A1569T

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.