Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.40 (T)

Chromosome 17:27782545 (forward strand) | View in location tab


with PhenCode NOS2:NM_000625.4:c.630+399G>A (C/T)

Most severe consequence
Evidence status


Archive dbSNP rs57224433

This variation has 3 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2647 individual genotypes and is mentioned in 5 citations.

Variation displays