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: 0.08 (T)
Location

Chromosome 11:2128765 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58739087

HGVS name

11:g.2128765C>T

This variation has assays on 5 chips - click the plus to show

Variation displays