Variant (rsID / SNP)

rs3738401

rs3738401 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DISC1. Location: chromosome 1, position 231,830,295. The table records no clinical significance for this variant.

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Reference-table entries

DISC1Not classified

Variant type: single nucleotide variant
Chromosome / position: 1:231830295
Cytoband: 1q42.2
HGVS: NM_018662.3(DISC1):c.791G>A (p.Arg264Gln)
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.