Original source

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

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

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

Co-located

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

Most severe consequence
Evidence status

Synonyms

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

Variation displays