Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.47 (A)
Location

Chromosome 19:34817436 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59522690

This variation has 2 HGVS names - click the plus to show

19:g.34817436A>T
ENST00000590963.1:n.798T>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays