Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.30 (G)
Location

Chromosome 12:48396450 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58887857, rs17119670

This variation has 6 HGVS names - click the plus to show

12:g.48396450G>T
ENST00000490609.1:n.250+1570C>A
ENST00000380518.3:c.85+1570C>A
ENST00000465743.2:n.501C>A
ENST00000337299.6:c.85+1570C>A
ENST00000474996.2:n.213+1570C>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays