Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.20 (T)
Location

Chromosome 11:5242453 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

11:g.5242453C>T
ENST00000454892.1:n.162-206G>A
ENST00000433329.1:n.312-206G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays