Variant (rsID / SNP)

rs1031688

rs1031688 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANK3. Location: chromosome 10, position 62,038,544. Clinical significance in the table: Benign.

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Reference-table entries

ANK3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:62038544
Cytoband: 10q21.2
HGVS: NM_020987.5(ANK3):c.402T>C (p.Asn134=)
Allele change: Synonymous_N134N

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.