Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.41 (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
Intron variant
Evidence status


Archive dbSNP rs57224433

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 2 transcripts, has 4048 sample genotypes and is mentioned in 5 citations.

Variant displays