Original source

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

Alleles
A/T | Ambiguity code: W | MAF: 0.34 (A)
Location

Chromosome 11:18264227 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60261995, rs52832266

HGVS name

11:g.18264227A>T

This variation has assays on 4 chips - click the plus to show

Variation displays