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Variant (rsID / SNP)

rs150534917

ARID1A

rs150534917 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARID1A. Location: chromosome 1, position 27,105,880. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ARID1AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:27105880
Cytoband
1p36.11
HGVS
NM_006015.6(ARID1A):c.5491C>G (p.Leu1831Val)
Allele change
Missense_L1614V

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.