Variant (rsID / SNP)

rs140285438

rs140285438 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARID2. Location: chromosome 12, position 46,205,208. Clinical significance in the table: Benign.

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Reference-table entries

ARID2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:46205208
Cytoband: 12q12
HGVS: NM_152641.4(ARID2):c.292G>A (p.Glu98Lys)
Allele change: Missense_E98K

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.